SNP Report

Basic Info

Name	rs138891 dbSNP Ensembl
Location	chr22:49834093 - 49834093(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.39996
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000565177); non_coding_transcript_variant(ENST00000565177)
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 rs138891 (count: 0) View in gBrowse (chr22:49834093..49834093 )

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

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