rs763975867

Orientation

plus

Stabilized

plus

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

Make rs763975867(A;A)

Make rs763975867(A;T)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

18148570

Gene	LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs763975867
dbSNP (classic)	rs763975867
ClinGen	rs763975867
ebi	rs763975867
HLI	rs763975867
Exac	rs763975867
Gnomad	rs763975867
Varsome	rs763975867
LitVar	rs763975867
Map	rs763975867
PheGenI	rs763975867
Biobank	rs763975867
1000 genomes	rs763975867
hgdp	rs763975867
ensembl	rs763975867
geneview	rs763975867
scholar	rs763975867
google	rs763975867
pharmgkb	rs763975867
gwascentral	rs763975867
openSNP	rs763975867
23andMe	rs763975867
SNPshot	rs763975867
SNPdbe	rs763975867
MSV3d	rs763975867
GWAS Ctlg	rs763975867

Max Magnitude

0

ClinVar
Risk	rs763975867(A;A)
Alt	rs763975867(A;A)
Reference	Rs763975867(T;T)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18051884T>A
CLNSRC
CLNACC	RCV000369680.1,