rs121908967

Orientation

plus

Stabilized

plus

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

Make rs121908967(A;T)

Make rs121908967(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18151859

Gene	LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs121908967
dbSNP (classic)	rs121908967
ClinGen	rs121908967
ebi	rs121908967
HLI	rs121908967
Exac	rs121908967
Gnomad	rs121908967
Varsome	rs121908967
LitVar	rs121908967
Map	rs121908967
PheGenI	rs121908967
Biobank	rs121908967
1000 genomes	rs121908967
hgdp	rs121908967
ensembl	rs121908967
geneview	rs121908967
scholar	rs121908967
google	rs121908967
pharmgkb	rs121908967
gwascentral	rs121908967
openSNP	rs121908967
23andMe	rs121908967
SNPshot	rs121908967
SNPdbe	rs121908967
MSV3d	rs121908967
GWAS Ctlg	rs121908967

Max Magnitude

0

OMIM	602666
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908967(T;T)
Alt	rs121908967(T;T)
Reference	Rs121908967(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18055173A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007367.2,