rs587776808

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar
(GA;GA)	0	common in clinvar
(I;I)	0	common genotype

Make rs587776808(-;-)

Make rs587776808(-;C)

Reference

GRCh38 38.1/142

Chromosome

22

Position

36282730

Gene

MYH9

is a	snp
is	mentioned by
dbSNP	rs587776808
dbSNP (classic)	rs587776808
ClinGen	rs587776808
ebi	rs587776808
HLI	rs587776808
Exac	rs587776808
Gnomad	rs587776808
Varsome	rs587776808
LitVar	rs587776808
Map	rs587776808
PheGenI	rs587776808
Biobank	rs587776808
1000 genomes	rs587776808
hgdp	rs587776808
ensembl	rs587776808
geneview	rs587776808
scholar	rs587776808
google	rs587776808
pharmgkb	rs587776808
gwascentral	rs587776808
openSNP	rs587776808
23andMe	rs587776808
SNPshot	rs587776808
SNPdbe	rs587776808
MSV3d	rs587776808
GWAS Ctlg	rs587776808

Max Magnitude

0

ClinVar
Risk	Rs587776808(C;C) rs587776808(-;-)
Alt	Rs587776808(C;C) rs587776808(-;-)
Reference	Rs587776808(G;G)
Significance	Pathogenic
Disease	May-Hegglin anomaly MYH9 related disorders
Variation	info
Gene	MYH9
CLNDBN	May-Hegglin anomaly MYH9 related disorders
Reversed	1
HGVS	NC_000022.10:g.36678776delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015131.26, RCV000192271.1,