SNP Report

Basic Info

Name	rs10778683 dbSNP Ensembl
Location	chr12:79630240 - 79630240(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.29972
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000328827, ENST00000549050, ENST00000550006, ENST00000551712); non_coding_transcript_variant(ENST00000549050, ENST00000550006)
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)
PAWR	PRKC, apoptosis, WT1, regulator	12q21.2	1(0/1/0)

SNPs in LD with rs10778683 (count: 0) View in gBrowse (chr12:79630240..79630240 )

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

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