rs377015931

Orientation

plus

Stabilized

plus

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

Make rs377015931(A;A)

Make rs377015931(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

18157155

Gene	LOC105371567, MYO15A

is a	snp
is	mentioned by
dbSNP	rs377015931
dbSNP (classic)	rs377015931
ClinGen	rs377015931
ebi	rs377015931
HLI	rs377015931
Exac	rs377015931
Gnomad	rs377015931
Varsome	rs377015931
LitVar	rs377015931
Map	rs377015931
PheGenI	rs377015931
Biobank	rs377015931
1000 genomes	rs377015931
hgdp	rs377015931
ensembl	rs377015931
geneview	rs377015931
scholar	rs377015931
google	rs377015931
pharmgkb	rs377015931
gwascentral	rs377015931
openSNP	rs377015931
23andMe	rs377015931
SNPshot	rs377015931
SNPdbe	rs377015931
MSV3d	rs377015931
GWAS Ctlg	rs377015931

Max Magnitude

0

ClinVar
Risk	rs377015931(A;A)
Alt	rs377015931(A;A)
Reference	Rs377015931(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness Deafness
Variation	info
Gene	MYO15A
CLNDBN	Nonsyndromic hearing loss and deafness Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18060469G>A
CLNSRC
CLNACC	RCV000155197.1, RCV000477929.1,