SNP Report

Basic Info

Name	rs16847357 dbSNP Ensembl
Location	chr2:211964772 - 211964772(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.137979
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000260943, ENST00000342788, ENST00000402597, ENST00000435846, ENST00000436443, ENST00000484594); non_coding_transcript_variant(ENST00000484594); upstream_gene_variant(ENST00000484474)
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)
ERBB4	erb-b2 receptor tyrosine kinase 4	2q33.3-q34	2(1/1/0)

SNPs in LD with rs16847357 (count: 0) View in gBrowse (chr2:211964772..211964772 )

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

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