rs267606903

Orientation

minus

Stabilized

minus

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

Make rs267606903(A;A)

Make rs267606903(A;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23394294

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs267606903
dbSNP (classic)	rs267606903
ClinGen	rs267606903
ebi	rs267606903
HLI	rs267606903
Exac	rs267606903
Gnomad	rs267606903
Varsome	rs267606903
LitVar	rs267606903
Map	rs267606903
PheGenI	rs267606903
Biobank	rs267606903
1000 genomes	rs267606903
hgdp	rs267606903
ensembl	rs267606903
geneview	rs267606903
scholar	rs267606903
google	rs267606903
pharmgkb	rs267606903
gwascentral	rs267606903
openSNP	rs267606903
23andMe	rs267606903
SNPshot	rs267606903
SNPdbe	rs267606903
MSV3d	rs267606903
GWAS Ctlg	rs267606903

Max Magnitude

0

ClinVar
Risk	rs267606903(A;A)
Alt	rs267606903(A;A)
Reference	Rs267606903(T;T)
Significance	Pathogenic
Disease	Atrial septal defect 3
Variation	info
Gene	MYH6
CLNDBN	Atrial septal defect 3
Reversed	1
HGVS	NC_000014.8:g.23863503A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015211.25,