rs41298135

Orientation

plus

Stabilized

plus

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

Make rs41298135(A;A)

Make rs41298135(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77158332

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs41298135
dbSNP (classic)	rs41298135
ClinGen	rs41298135
ebi	rs41298135
HLI	rs41298135
Exac	rs41298135
Gnomad	rs41298135
Varsome	rs41298135
LitVar	rs41298135
Map	rs41298135
PheGenI	rs41298135
Biobank	rs41298135
1000 genomes	rs41298135
hgdp	rs41298135
ensembl	rs41298135
geneview	rs41298135
scholar	rs41298135
google	rs41298135
pharmgkb	rs41298135
gwascentral	rs41298135
openSNP	rs41298135
23andMe	rs41298135
SNPshot	rs41298135
SNPdbe	rs41298135
MSV3d	rs41298135
GWAS Ctlg	rs41298135

GMAF

0.001377

Max Magnitude

0

OMIM	276903
Desc
Variant	0006
Related	also

ClinVar
Risk	rs41298135(A;A) rs41298135(T;T)
Alt	rs41298135(A;A) rs41298135(T;T)
Reference	Rs41298135(G;G)
Significance	Other
Disease	Usher syndrome not specified Nonsyndromic Hearing Loss Nonsyndromic Hearing Loss Retinitis pigmentosa-deafness syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1B not specified Nonsyndromic Hearing Loss, Dominant Nonsyndromic Hearing Loss, Recessive Retinitis pigmentosa-deafness syndrome
Reversed	0
HGVS	NC_000011.9:g.76869378G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012626.19, RCV000036251.3, RCV000282374.1, RCV000337254.1, RCV000386045.1,