rs765468034

Orientation

plus

Stabilized

plus

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

Make rs765468034(C;T)

Make rs765468034(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

18142826

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs765468034
dbSNP (classic)	rs765468034
ClinGen	rs765468034
ebi	rs765468034
HLI	rs765468034
Exac	rs765468034
Gnomad	rs765468034
Varsome	rs765468034
LitVar	rs765468034
Map	rs765468034
PheGenI	rs765468034
Biobank	rs765468034
1000 genomes	rs765468034
hgdp	rs765468034
ensembl	rs765468034
geneview	rs765468034
scholar	rs765468034
google	rs765468034
pharmgkb	rs765468034
gwascentral	rs765468034
openSNP	rs765468034
23andMe	rs765468034
SNPshot	rs765468034
SNPdbe	rs765468034
MSV3d	rs765468034
GWAS Ctlg	rs765468034

Max Magnitude

0

ClinVar
Risk	rs765468034(T;T)
Alt	rs765468034(T;T)
Reference	Rs765468034(C;C)
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.18046140C>T
CLNSRC
CLNACC	RCV000214976.1,