rs201023600

Orientation

plus

Stabilized

plus

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

Make rs201023600(A;A)

Make rs201023600(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

26147429

Gene

MYO3A

is a	snp
is	mentioned by
dbSNP	rs201023600
dbSNP (classic)	rs201023600
ClinGen	rs201023600
ebi	rs201023600
HLI	rs201023600
Exac	rs201023600
Gnomad	rs201023600
Varsome	rs201023600
LitVar	rs201023600
Map	rs201023600
PheGenI	rs201023600
Biobank	rs201023600
1000 genomes	rs201023600
hgdp	rs201023600
ensembl	rs201023600
geneview	rs201023600
scholar	rs201023600
google	rs201023600
pharmgkb	rs201023600
gwascentral	rs201023600
openSNP	rs201023600
23andMe	rs201023600
SNPshot	rs201023600
SNPdbe	rs201023600
MSV3d	rs201023600
GWAS Ctlg	rs201023600

Max Magnitude

0

ClinVar
Risk	rs201023600(A;A)
Alt	rs201023600(A;A)
Reference	Rs201023600(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO3A
CLNDBN	Deafness, autosomal recessive 30
Reversed	0
HGVS	NC_000010.10:g.26436358G>A
CLNSRC
CLNACC	RCV000290723.1,