rs797044804

Orientation

minus

Stabilized

minus

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

Make rs797044804(A;T)

Make rs797044804(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

36291990

Gene

MYH9

is a	snp
is	mentioned by
dbSNP	rs797044804
dbSNP (classic)	rs797044804
ClinGen	rs797044804
ebi	rs797044804
HLI	rs797044804
Exac	rs797044804
Gnomad	rs797044804
Varsome	rs797044804
LitVar	rs797044804
Map	rs797044804
PheGenI	rs797044804
Biobank	rs797044804
1000 genomes	rs797044804
hgdp	rs797044804
ensembl	rs797044804
geneview	rs797044804
scholar	rs797044804
google	rs797044804
pharmgkb	rs797044804
gwascentral	rs797044804
openSNP	rs797044804
23andMe	rs797044804
SNPshot	rs797044804
SNPdbe	rs797044804
MSV3d	rs797044804
GWAS Ctlg	rs797044804

Max Magnitude

0

ClinVar
Risk	rs797044804(T;T)
Alt	rs797044804(T;T)
Reference	Rs797044804(A;A)
Significance	Pathogenic
Disease	MYH9 related disorders
Variation	info
Gene	MYH9
CLNDBN	MYH9 related disorders
Reversed	1
HGVS	NC_000022.10:g.36688036T>A
CLNSRC
CLNACC	RCV000192270.1,