rs878853225

Orientation

plus

Stabilized

plus

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

Make rs878853225(C;C)

Make rs878853225(C;GGT)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

75858993

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs878853225
dbSNP (classic)	rs878853225
ClinGen	rs878853225
ebi	rs878853225
HLI	rs878853225
Exac	rs878853225
Gnomad	rs878853225
Varsome	rs878853225
LitVar	rs878853225
Map	rs878853225
PheGenI	rs878853225
Biobank	rs878853225
1000 genomes	rs878853225
hgdp	rs878853225
ensembl	rs878853225
geneview	rs878853225
scholar	rs878853225
google	rs878853225
pharmgkb	rs878853225
gwascentral	rs878853225
openSNP	rs878853225
23andMe	rs878853225
SNPshot	rs878853225
SNPdbe	rs878853225
MSV3d	rs878853225
GWAS Ctlg	rs878853225

Max Magnitude

0

ClinVar
Risk	rs878853225(C;C)
Alt	rs878853225(C;C)
Reference	Rs878853225(GGT;GGT)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO6
CLNDBN	Deafness, autosomal dominant 22
Reversed	0
HGVS	NC_000006.11:g.76568710_76568712delGGTinsC
CLNSRC
CLNACC	RCV000225059.1,