SNP Report

Basic Info

Name	rs12769628 dbSNP Ensembl
Location	chr10:67968862 - 67968862(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.105232
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000277817, ENST00000373700, ENST00000395198, ENST00000412272, ENST00000427635, ENST00000460168, ENST00000473533); NMD_transcript_variant(ENST00000427635, ENST00000473533); non_coding_transcript_variant(ENST00000460168)
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)
HERC4	HECT and RLD domain containing E3 ubiquitin protein ligase 4	10q21.3	Mapped by Literature SNP

SNPs in LD with rs12769628 (count: 0) View in gBrowse (chr10:67968862..67968862 )

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

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