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rs149585781

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149585781(A;A)
Make rs149585781(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position39666063
GenePNMT, TCAP
is asnp
is mentioned by
dbSNPrs149585781
ebirs149585781
HLIrs149585781
Exacrs149585781
Varsomers149585781
Maprs149585781
PheGenIrs149585781
hapmaprs149585781
1000 genomesrs149585781
hgdprs149585781
ensemblrs149585781
gopubmedrs149585781
geneviewrs149585781
scholarrs149585781
googlers149585781
pharmgkbrs149585781
gwascentralrs149585781
openSNPrs149585781
23andMers149585781
23andMe allrs149585781
SNP Nexus

SNPshotrs149585781
SNPdbers149585781
MSV3drs149585781
GWAS Ctlgrs149585781
Max Magnitude0
ClinVar
Risk rs149585781(A;A)
Alt rs149585781(A;A)
Reference rs149585781(G;G)
Significance Pathogenic
Disease not specified Dilated cardiomyopathy 1N
Variation info
Gene TCAP PNMT
CLNDBN not specified Dilated cardiomyopathy 1N
Reversed 0
HGVS NC_000017.10:g.37822316G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000037797.4, RCV000170302.4,