rs121908966

Orientation

plus

Stabilized

plus

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

Make rs121908966(A;T)

Make rs121908966(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18145929

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs121908966
dbSNP (classic)	rs121908966
ClinGen	rs121908966
ebi	rs121908966
HLI	rs121908966
Exac	rs121908966
Gnomad	rs121908966
Varsome	rs121908966
LitVar	rs121908966
Map	rs121908966
PheGenI	rs121908966
Biobank	rs121908966
1000 genomes	rs121908966
hgdp	rs121908966
ensembl	rs121908966
geneview	rs121908966
scholar	rs121908966
google	rs121908966
pharmgkb	rs121908966
gwascentral	rs121908966
openSNP	rs121908966
23andMe	rs121908966
SNPshot	rs121908966
SNPdbe	rs121908966
MSV3d	rs121908966
GWAS Ctlg	rs121908966

Max Magnitude

0

OMIM	602666
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908966(T;T)
Alt	rs121908966(T;T)
Reference	Rs121908966(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18049243A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007366.2,