rs199621031

Orientation

plus

Stabilized

plus

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

Make rs199621031(A;A)

Make rs199621031(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

18163251

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs199621031
dbSNP (classic)	rs199621031
ClinGen	rs199621031
ebi	rs199621031
HLI	rs199621031
Exac	rs199621031
Gnomad	rs199621031
Varsome	rs199621031
LitVar	rs199621031
Map	rs199621031
PheGenI	rs199621031
Biobank	rs199621031
1000 genomes	rs199621031
hgdp	rs199621031
ensembl	rs199621031
geneview	rs199621031
scholar	rs199621031
google	rs199621031
pharmgkb	rs199621031
gwascentral	rs199621031
openSNP	rs199621031
23andMe	rs199621031
SNPshot	rs199621031
SNPdbe	rs199621031
MSV3d	rs199621031
GWAS Ctlg	rs199621031

Max Magnitude

0

ClinVar
Risk	rs199621031(A;A)
Alt	rs199621031(A;A)
Reference	Rs199621031(G;G)
Significance	Probable-Pathogenic
Disease	not specified Nonsyndromic Hearing Loss not provided
Variation	info
Gene	MYO15A
CLNDBN	not specified Nonsyndromic Hearing Loss, Recessive not provided
Reversed	0
HGVS	NC_000017.10:g.18066565G>A
CLNSRC
CLNACC	RCV000217646.1, RCV000326631.1, RCV000413658.1,