SNP Report

Basic Info

Name	rs17109234 dbSNP Ensembl
Location	chr12:71061920 - 71061920(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.0407348
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000548497, ENST00000549357); non_coding_transcript_variant(ENST00000548497, ENST00000549357)
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 rs17109234 (count: 0) View in gBrowse (chr12:71061920..71061920 )

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

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