rs886042860

Orientation

plus

Stabilized

plus

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

Chromosome

10

Position

26173711

Gene

MYO3A

is a	snp
is	mentioned by
dbSNP	rs886042860
dbSNP (classic)	rs886042860
ClinGen	rs886042860
ebi	rs886042860
HLI	rs886042860
Exac	rs886042860
Gnomad	rs886042860
Varsome	rs886042860
LitVar	rs886042860
Map	rs886042860
PheGenI	rs886042860
Biobank	rs886042860
1000 genomes	rs886042860
hgdp	rs886042860
ensembl	rs886042860
geneview	rs886042860
scholar	rs886042860
google	rs886042860
pharmgkb	rs886042860
gwascentral	rs886042860
openSNP	rs886042860
23andMe	rs886042860
SNPshot	rs886042860
SNPdbe	rs886042860
MSV3d	rs886042860
GWAS Ctlg	rs886042860

Max Magnitude

0

ClinVar
Risk	rs886042860(-;-)
Alt	rs886042860(-;-)
Reference	Rs886042860(AA;AA)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO3A
CLNDBN	Deafness, autosomal recessive 30
Reversed	0
HGVS	NC_000010.10:g.26462640_26462641delAA
CLNSRC
CLNACC	RCV000309682.1,