rs121912559

Orientation

plus

Stabilized

plus

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

Make rs121912559(A;T)

Make rs121912559(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

75840678

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs121912559
dbSNP (classic)	rs121912559
ClinGen	rs121912559
ebi	rs121912559
HLI	rs121912559
Exac	rs121912559
Gnomad	rs121912559
Varsome	rs121912559
LitVar	rs121912559
Map	rs121912559
PheGenI	rs121912559
Biobank	rs121912559
1000 genomes	rs121912559
hgdp	rs121912559
ensembl	rs121912559
geneview	rs121912559
scholar	rs121912559
google	rs121912559
pharmgkb	rs121912559
gwascentral	rs121912559
openSNP	rs121912559
23andMe	rs121912559
SNPshot	rs121912559
SNPdbe	rs121912559
MSV3d	rs121912559
GWAS Ctlg	rs121912559

Merged from

Rs28936390

Max Magnitude

0

OMIM	600970
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121912559(T;T)
Alt	rs121912559(T;T)
Reference	Rs121912559(A;A)
Significance	Pathogenic
Disease	Deafness not specified
Variation	info
Gene	MYO6
CLNDBN	Deafness, autosomal recessive 37 not specified
Reversed	0
HGVS	NC_000006.11:g.76550395A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009111.2, RCV000154352.1,