rs149585781

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs149585781(A;A)

Make rs149585781(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

39666063

Gene	PNMT, TCAP

is a	snp
is	mentioned by
dbSNP	rs149585781
dbSNP (classic)	rs149585781
ClinGen	rs149585781
ebi	rs149585781
HLI	rs149585781
Exac	rs149585781
Gnomad	rs149585781
Varsome	rs149585781
LitVar	rs149585781
Map	rs149585781
PheGenI	rs149585781
Biobank	rs149585781
1000 genomes	rs149585781
hgdp	rs149585781
ensembl	rs149585781
geneview	rs149585781
scholar	rs149585781
google	rs149585781
pharmgkb	rs149585781
gwascentral	rs149585781
openSNP	rs149585781
23andMe	rs149585781
SNPshot	rs149585781
SNPdbe	rs149585781
MSV3d	rs149585781
GWAS Ctlg	rs149585781

Max Magnitude

0

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 UniProtKB (protein)
CLNACC	RCV000037797.5, RCV000170302.4,