rs33962952

Orientation

plus

Stabilized

plus

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

Make rs33962952(C;T)

Make rs33962952(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

57037618

Gene

MYO1A

is a	snp
is	mentioned by
dbSNP	rs33962952
dbSNP (classic)	rs33962952
ClinGen	rs33962952
ebi	rs33962952
HLI	rs33962952
Exac	rs33962952
Gnomad	rs33962952
Varsome	rs33962952
LitVar	rs33962952
Map	rs33962952
PheGenI	rs33962952
Biobank	rs33962952
1000 genomes	rs33962952
hgdp	rs33962952
ensembl	rs33962952
geneview	rs33962952
scholar	rs33962952
google	rs33962952
pharmgkb	rs33962952
gwascentral	rs33962952
openSNP	rs33962952
23andMe	rs33962952
SNPshot	rs33962952
SNPdbe	rs33962952
MSV3d	rs33962952
GWAS Ctlg	rs33962952

GMAF

0.01469

Max Magnitude

0

OMIM	601478
Desc
Variant	0005
Related	also

ClinVar
Risk	rs33962952(T;T)
Alt	rs33962952(T;T)
Reference	Rs33962952(C;C)
Significance	Probable-non-pathogenic
Disease	Deafness not specified Nonsyndromic Hearing Loss
Variation	info
Gene	MYO1A
CLNDBN	Deafness, autosomal dominant 48 not specified Nonsyndromic Hearing Loss, Dominant
Reversed	0
HGVS	NC_000012.11:g.57431402C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008627.4, RCV000038471.3, RCV000369472.1,