rs876657709

Orientation

plus

Stabilized

plus

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

Make rs876657709(-;-)

Make rs876657709(-;AA)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

75890212

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs876657709
dbSNP (classic)	rs876657709
ClinGen	rs876657709
ebi	rs876657709
HLI	rs876657709
Exac	rs876657709
Gnomad	rs876657709
Varsome	rs876657709
LitVar	rs876657709
Map	rs876657709
PheGenI	rs876657709
Biobank	rs876657709
1000 genomes	rs876657709
hgdp	rs876657709
ensembl	rs876657709
geneview	rs876657709
scholar	rs876657709
google	rs876657709
pharmgkb	rs876657709
gwascentral	rs876657709
openSNP	rs876657709
23andMe	rs876657709
SNPshot	rs876657709
SNPdbe	rs876657709
MSV3d	rs876657709
GWAS Ctlg	rs876657709

Max Magnitude

0

ClinVar
Risk	rs876657709(-;-)
Alt	rs876657709(-;-)
Reference	Rs876657709(AA;AA)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO6
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000006.11:g.76599929_76599930delAA
CLNSRC
CLNACC	RCV000223613.1,