rs2856655

Orientation

minus

Stabilized

minus

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

Make rs2856655(A;A)

Make rs2856655(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

47337534

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs2856655
dbSNP (classic)	rs2856655
ClinGen	rs2856655
ebi	rs2856655
HLI	rs2856655
Exac	rs2856655
Gnomad	rs2856655
Varsome	rs2856655
LitVar	rs2856655
Map	rs2856655
PheGenI	rs2856655
Biobank	rs2856655
1000 genomes	rs2856655
hgdp	rs2856655
ensembl	rs2856655
geneview	rs2856655
scholar	rs2856655
google	rs2856655
pharmgkb	rs2856655
gwascentral	rs2856655
openSNP	rs2856655
23andMe	rs2856655
SNPshot	rs2856655
SNPdbe	rs2856655
MSV3d	rs2856655
GWAS Ctlg	rs2856655

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

OMIM	600958
Desc
Variant	0015
Related	also

ClinVar
Risk	rs2856655(A;A) rs2856655(C;C)
Alt	rs2856655(A;A) rs2856655(C;C)
Reference	Rs2856655(G;G)
Significance	Pathogenic
Disease	not provided Familial hypertrophic cardiomyopathy 4 not specified Primary familial hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	not provided Familial hypertrophic cardiomyopathy 4 not specified Primary familial hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000011.9:g.47359085C>G; NC_000011.9:g.47359085C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000158160.2, RCV000009148.6, RCV000158159.3, RCV000168802.2, RCV000211727.1,