SNP Report

Basic Info

Name	rs1509674 dbSNP Ensembl
Location	chr12:102179097 - 102179097(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.384185
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000327680, ENST00000392911, ENST00000412715, ENST00000417507, ENST00000457614, ENST00000535811, ENST00000541394, ENST00000543784); NMD_transcript_variant(ENST00000457614); non_coding_transcript_variant(ENST00000535811)
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)
PARPBP	PARP1 binding protein	12q23.2	Mapped by LD-proxy

SNPs in LD with rs1509674 (count: 0) View in gBrowse (chr12:102179097..102179097 )

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

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