rs712270

Orientation

minus

Stabilized

minus

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

Make rs712270(A;A)

Make rs712270(A;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

18153853

Gene	LOC105371567, LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs712270
dbSNP (classic)	rs712270
ClinGen	rs712270
ebi	rs712270
HLI	rs712270
Exac	rs712270
Gnomad	rs712270
Varsome	rs712270
LitVar	rs712270
Map	rs712270
PheGenI	rs712270
Biobank	rs712270
1000 genomes	rs712270
hgdp	rs712270
ensembl	rs712270
geneview	rs712270
scholar	rs712270
google	rs712270
pharmgkb	rs712270
gwascentral	rs712270
openSNP	rs712270
23andMe	rs712270
SNPshot	rs712270
SNPdbe	rs712270
MSV3d	rs712270
GWAS Ctlg	rs712270

GMAF

0.2466

Max Magnitude

0

?	(A;A) (A;T) (T;T)	28

ClinVar
Risk	rs712270(A;A)
Alt	rs712270(A;A)
Reference	Rs712270(T;T)
Significance	Probable-non-pathogenic
Disease	not specified Nonsyndromic Hearing Loss
Variation	info
Gene	MYO15A
CLNDBN	not specified Nonsyndromic Hearing Loss, Recessive
Reversed	1
HGVS	NC_000017.10:g.18057167A>T
CLNSRC
CLNACC	RCV000214657.2, RCV000317870.1,