SNP Report

Basic Info

Name	rs10861124 dbSNP Ensembl
Location	chr12:103859161 - 103859161(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.170527
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000548527, ENST00000551270); non_coding_transcript_variant(ENST00000548527, ENST00000551270)
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 rs10861124 (count: 0) View in gBrowse (chr12:103859161..103859161 )

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

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