rs397517045

Orientation

plus

Stabilized

plus

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

Make rs397517045(-;G)

Make rs397517045(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

75879853

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs397517045
dbSNP (classic)	rs397517045
ClinGen	rs397517045
ebi	rs397517045
HLI	rs397517045
Exac	rs397517045
Gnomad	rs397517045
Varsome	rs397517045
LitVar	rs397517045
Map	rs397517045
PheGenI	rs397517045
Biobank	rs397517045
1000 genomes	rs397517045
hgdp	rs397517045
ensembl	rs397517045
geneview	rs397517045
scholar	rs397517045
google	rs397517045
pharmgkb	rs397517045
gwascentral	rs397517045
openSNP	rs397517045
23andMe	rs397517045
SNPshot	rs397517045
SNPdbe	rs397517045
MSV3d	rs397517045
GWAS Ctlg	rs397517045

Max Magnitude

0

ClinVar
Risk	rs397517045(G;G)
Alt	rs397517045(G;G)
Reference	Rs397517045(-;-)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO6
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000006.11:g.76589570dupG
CLNSRC	ClinVar
CLNACC	RCV000038290.2,