SNP Report

Basic Info
Name rs76869876 dbSNP Ensembl
Location chr19:8949151 - 8949151(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.00579073
Functional Annotation missense_variant.
Polyphen Annotation: unknown(ENST00000397910)
Consequence to Transcript missense_variant(ENST00000397910)
No. of Studies 1 (Positive: 0; Negative: 0; Trend: 1)
Source Literature
Overlap with SZ? NO
Overlap with MDD? NO

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Georgi, B., 2014 A/G 7 in BPI, 4 in Well 7 in BPI, 4 in Well Top 30 Amish-specific putative damaging exonic missense vari...... Top 30 Amish-specific putative damaging exonic missense variants by prevalence in affected individuals. More... Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
MUC16 mucin 16, cell surface associated 19p13.2 1(0/0/1)

SNPs in LD with rs76869876 (count: 0) View in gBrowse (chr19:8949151..8949151 )

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

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