rs80338830

Orientation

minus

Stabilized

minus

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

Make rs80338830(G;T)

Make rs80338830(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

36295068

Gene

MYH9

is a	snp
is	mentioned by
dbSNP	rs80338830
dbSNP (classic)	rs80338830
ClinGen	rs80338830
ebi	rs80338830
HLI	rs80338830
Exac	rs80338830
Gnomad	rs80338830
Varsome	rs80338830
LitVar	rs80338830
Map	rs80338830
PheGenI	rs80338830
Biobank	rs80338830
1000 genomes	rs80338830
hgdp	rs80338830
ensembl	rs80338830
geneview	rs80338830
scholar	rs80338830
google	rs80338830
pharmgkb	rs80338830
gwascentral	rs80338830
openSNP	rs80338830
23andMe	rs80338830
SNPshot	rs80338830
SNPdbe	rs80338830
MSV3d	rs80338830
GWAS Ctlg	rs80338830

Max Magnitude

0

ClinVar
Risk	rs80338830(T;T)
Alt	rs80338830(T;T)
Reference	Rs80338830(G;G)
Significance	Pathogenic
Disease	MYH9 related disorders
Variation	info
Gene	MYH9
CLNDBN	MYH9 related disorders
Reversed	1
HGVS	NC_000022.10:g.36691114C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000032221.1,