rs55679042

Orientation

plus

Stabilized

plus

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

Make rs55679042(A;A)

Make rs55679042(A;G)

Make rs55679042(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

57043335

Gene

MYO1A

is a	snp
is	mentioned by
dbSNP	rs55679042
dbSNP (classic)	rs55679042
ClinGen	rs55679042
ebi	rs55679042
HLI	rs55679042
Exac	rs55679042
Gnomad	rs55679042
Varsome	rs55679042
LitVar	rs55679042
Map	rs55679042
PheGenI	rs55679042
Biobank	rs55679042
1000 genomes	rs55679042
hgdp	rs55679042
ensembl	rs55679042
geneview	rs55679042
scholar	rs55679042
google	rs55679042
pharmgkb	rs55679042
gwascentral	rs55679042
openSNP	rs55679042
23andMe	rs55679042
SNPshot	rs55679042
SNPdbe	rs55679042
MSV3d	rs55679042
GWAS Ctlg	rs55679042

GMAF

0.002296

Max Magnitude

0

OMIM	601478
Desc
Variant	0003
Related	also

ClinVar
Risk	rs55679042(T;T)
Alt	rs55679042(T;T)
Reference	Rs55679042(C;C)
Significance	Other
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.57437119C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008625.4, RCV000038478.3, RCV000348646.1,