SNP Report

Basic Info

Name	rs12949747 dbSNP Ensembl
Location	chr17:30257340 - 30257340(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.252396
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000261714, ENST00000578090); NMD_transcript_variant(ENST00000578090)
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)
BLMH	bleomycin hydrolase	17q11.2	Mapped by Literature SNP

SNPs in LD with rs12949747 (count: 0) View in gBrowse (chr17:30257340..30257340 )

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

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