BDgene

SNP Report

Basic Info
Name rs6922302 dbSNP Ensembl
Location chr6:28327533 - 28327533(1)
Variant Alleles C/G
Ancestral Allele C
Minor Allele G
Minor Allele Frequence 0.0519169
Functional Annotation 5_prime_UTR_variant; downstream_gene_variant; missense_variant; splice_region_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000439636, ENST00000453745, ENST00000344279, ENST00000396838, ENST00000414429, ENST00000439158, ENST00000447021); possibly damaging(ENST00000426434)
SIFT Annotation: deleterious - low confidence(ENST00000426434); tolerated(ENST00000344279, ENST00000396838, ENST00000414429, ENST00000439158, ENST00000447021); deleterious(ENST00000439636, ENST00000453745)
Consequence to Transcript 5_prime_UTR_variant(ENST00000414431, ENST00000435857, ENST00000446474, ENST00000611469); downstream_gene_variant(ENST00000426756, ENST00000434036, ENST00000439628, ENST00000444081, ENST00000446222); missense_variant(ENST00000439636, ENST00000453745, ENST00000344279, ENST00000396838, ENST00000414429, ENST00000439158, ENST00000447021, ENST00000426434); splice_region_variant(ENST00000439636, ENST00000453745, ENST00000344279, ENST00000396838, ENST00000414429, ENST00000439158, ENST00000447021, ENST00000414431, ENST00000435857, ENST00000446474, ENST00000611469, ENST00000426434); upstream_gene_variant(ENST00000481934)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
ZSCAN31 zinc finger and SCAN domain containing 31 6p 1(1/0/0)

SNPs in LD with rs6922302 (count: 0) View in gBrowse (chr6:28327533..28327533 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)