rs727503284

Orientation

minus

Stabilized

minus

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

Make rs727503284(G;T)

Make rs727503284(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

36289096

Gene

MYH9

is a	snp
is	mentioned by
dbSNP	rs727503284
dbSNP (classic)	rs727503284
ClinGen	rs727503284
ebi	rs727503284
HLI	rs727503284
Exac	rs727503284
Gnomad	rs727503284
Varsome	rs727503284
LitVar	rs727503284
Map	rs727503284
PheGenI	rs727503284
Biobank	rs727503284
1000 genomes	rs727503284
hgdp	rs727503284
ensembl	rs727503284
geneview	rs727503284
scholar	rs727503284
google	rs727503284
pharmgkb	rs727503284
gwascentral	rs727503284
openSNP	rs727503284
23andMe	rs727503284
SNPshot	rs727503284
SNPdbe	rs727503284
MSV3d	rs727503284
GWAS Ctlg	rs727503284

Max Magnitude

0

ClinVar
Risk	rs727503284(T;T)
Alt	rs727503284(T;T)
Reference	Rs727503284(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYH9
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000022.10:g.36685142C>A
CLNSRC
CLNACC	RCV000151326.1,