SNP Report

Basic Info

Name	rs1381171 dbSNP Ensembl
Location	chr1:60576926 - 60576926(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.405351
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000439156, ENST00000634281, ENST00000634836, ENST00000635048, ENST00000635616); non_coding_transcript_variant(ENST00000439156, ENST00000634281, ENST00000634836, ENST00000635048, ENST00000635616)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs1381171 (count: 0) View in gBrowse (chr1:60576926..60576926 )

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

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