rs771297865

Orientation

plus

Stabilized

plus

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

Make rs771297865(C;T)

Make rs771297865(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

15737617

Gene

MYH11

is a	snp
is	mentioned by
dbSNP	rs771297865
dbSNP (classic)	rs771297865
ClinGen	rs771297865
ebi	rs771297865
HLI	rs771297865
Exac	rs771297865
Gnomad	rs771297865
Varsome	rs771297865
LitVar	rs771297865
Map	rs771297865
PheGenI	rs771297865
Biobank	rs771297865
1000 genomes	rs771297865
hgdp	rs771297865
ensembl	rs771297865
geneview	rs771297865
scholar	rs771297865
google	rs771297865
pharmgkb	rs771297865
gwascentral	rs771297865
openSNP	rs771297865
23andMe	rs771297865
SNPshot	rs771297865
SNPdbe	rs771297865
MSV3d	rs771297865
GWAS Ctlg	rs771297865

Max Magnitude

0

ClinVar
Risk	rs771297865(T;T)
Alt	rs771297865(T;T)
Reference	Rs771297865(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH11
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.15831474C>T
CLNSRC
CLNACC	RCV000182502.2,