rs876657707

Orientation

plus

Stabilized

plus

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

Make rs876657707(-;C)

Make rs876657707(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

18119985

Gene	LOC105371566, MYO15A

is a	snp
is	mentioned by
dbSNP	rs876657707
dbSNP (classic)	rs876657707
ClinGen	rs876657707
ebi	rs876657707
HLI	rs876657707
Exac	rs876657707
Gnomad	rs876657707
Varsome	rs876657707
LitVar	rs876657707
Map	rs876657707
PheGenI	rs876657707
Biobank	rs876657707
1000 genomes	rs876657707
hgdp	rs876657707
ensembl	rs876657707
geneview	rs876657707
scholar	rs876657707
google	rs876657707
pharmgkb	rs876657707
gwascentral	rs876657707
openSNP	rs876657707
23andMe	rs876657707
SNPshot	rs876657707
SNPdbe	rs876657707
MSV3d	rs876657707
GWAS Ctlg	rs876657707

Max Magnitude

0

ClinVar
Risk	rs876657707(C;C)
Alt	rs876657707(C;C)
Reference	Rs876657707(-;-)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO15A
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000017.10:g.18023299dupC
CLNSRC
CLNACC	RCV000223213.1,