SNP Report

Basic Info

Name	rs10861671 dbSNP Ensembl
Location	chr12:106827149 - 106827149(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.341054
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000355478, ENST00000392837, ENST00000392839, ENST00000462949, ENST00000470628, ENST00000470960, ENST00000548914, ENST00000549643); NMD_transcript_variant(ENST00000462949, ENST00000470960); non_coding_transcript_variant(ENST00000470628)
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)
RIC8B	RIC8 guanine nucleotide exchange factor B	12q23.3	Mapped by LD-proxy

SNPs in LD with rs10861671 (count: 0) View in gBrowse (chr12:106827149..106827149 )

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

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