rs121965084

Orientation

plus

Stabilized

plus

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

Make rs121965084(A;T)

Make rs121965084(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77162149

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs121965084
dbSNP (classic)	rs121965084
ClinGen	rs121965084
ebi	rs121965084
HLI	rs121965084
Exac	rs121965084
Gnomad	rs121965084
Varsome	rs121965084
LitVar	rs121965084
Map	rs121965084
PheGenI	rs121965084
Biobank	rs121965084
1000 genomes	rs121965084
hgdp	rs121965084
ensembl	rs121965084
geneview	rs121965084
scholar	rs121965084
google	rs121965084
pharmgkb	rs121965084
gwascentral	rs121965084
openSNP	rs121965084
23andMe	rs121965084
SNPshot	rs121965084
SNPdbe	rs121965084
MSV3d	rs121965084
GWAS Ctlg	rs121965084

Merged from

Rs28934903

Max Magnitude

0

OMIM	276903
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121965084(G;G) rs121965084(T;T)
Alt	rs121965084(G;G) rs121965084(T;T)
Reference	Rs121965084(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal dominant 11
Reversed	0
HGVS	NC_000011.9:g.76873195A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012638.19,