rs121908968

Orientation

plus

Stabilized

plus

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

Make rs121908968(C;T)

Make rs121908968(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18124558

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs121908968
dbSNP (classic)	rs121908968
ClinGen	rs121908968
ebi	rs121908968
HLI	rs121908968
Exac	rs121908968
Gnomad	rs121908968
Varsome	rs121908968
LitVar	rs121908968
Map	rs121908968
PheGenI	rs121908968
Biobank	rs121908968
1000 genomes	rs121908968
hgdp	rs121908968
ensembl	rs121908968
geneview	rs121908968
scholar	rs121908968
google	rs121908968
pharmgkb	rs121908968
gwascentral	rs121908968
openSNP	rs121908968
23andMe	rs121908968
SNPshot	rs121908968
SNPdbe	rs121908968
MSV3d	rs121908968
GWAS Ctlg	rs121908968

Max Magnitude

0

OMIM	602666
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908968(T;T)
Alt	rs121908968(T;T)
Reference	Rs121908968(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18027872C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007368.2,