rs121908965

Orientation

plus

Stabilized

plus

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

Make rs121908965(A;T)

Make rs121908965(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18145935

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs121908965
dbSNP (classic)	rs121908965
ClinGen	rs121908965
ebi	rs121908965
HLI	rs121908965
Exac	rs121908965
Gnomad	rs121908965
Varsome	rs121908965
LitVar	rs121908965
Map	rs121908965
PheGenI	rs121908965
Biobank	rs121908965
1000 genomes	rs121908965
hgdp	rs121908965
ensembl	rs121908965
geneview	rs121908965
scholar	rs121908965
google	rs121908965
pharmgkb	rs121908965
gwascentral	rs121908965
openSNP	rs121908965
23andMe	rs121908965
SNPshot	rs121908965
SNPdbe	rs121908965
MSV3d	rs121908965
GWAS Ctlg	rs121908965

Max Magnitude

0

OMIM	602666
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908965(T;T)
Alt	rs121908965(T;T)
Reference	Rs121908965(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18049249A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007365.2,