rs370310929

Orientation

plus

Stabilized

plus

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

Make rs370310929(A;A)

Make rs370310929(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23429047

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs370310929
dbSNP (classic)	rs370310929
ClinGen	rs370310929
ebi	rs370310929
HLI	rs370310929
Exac	rs370310929
Gnomad	rs370310929
Varsome	rs370310929
LitVar	rs370310929
Map	rs370310929
PheGenI	rs370310929
Biobank	rs370310929
1000 genomes	rs370310929
hgdp	rs370310929
ensembl	rs370310929
geneview	rs370310929
scholar	rs370310929
google	rs370310929
pharmgkb	rs370310929
gwascentral	rs370310929
openSNP	rs370310929
23andMe	rs370310929
SNPshot	rs370310929
SNPdbe	rs370310929
MSV3d	rs370310929
GWAS Ctlg	rs370310929

Max Magnitude

0

ClinVar
Risk	rs370310929(A;A) rs370310929(C;C)
Alt	rs370310929(A;A) rs370310929(C;C)
Reference	Rs370310929(T;T)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	0
HGVS	NC_000014.8:g.23898256T>A; NC_000014.8:g.23898256T>C
CLNSRC
CLNACC	RCV000154611.2, RCV000158793.2,