rs727503326

Orientation

plus

Stabilized

plus

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

Make rs727503326(C;T)

Make rs727503326(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

75844906

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs727503326
dbSNP (classic)	rs727503326
ClinGen	rs727503326
ebi	rs727503326
HLI	rs727503326
Exac	rs727503326
Gnomad	rs727503326
Varsome	rs727503326
LitVar	rs727503326
Map	rs727503326
PheGenI	rs727503326
Biobank	rs727503326
1000 genomes	rs727503326
hgdp	rs727503326
ensembl	rs727503326
geneview	rs727503326
scholar	rs727503326
google	rs727503326
pharmgkb	rs727503326
gwascentral	rs727503326
openSNP	rs727503326
23andMe	rs727503326
SNPshot	rs727503326
SNPdbe	rs727503326
MSV3d	rs727503326
GWAS Ctlg	rs727503326

Max Magnitude

0

ClinVar
Risk	rs727503326(T;T)
Alt	rs727503326(T;T)
Reference	Rs727503326(C;C)
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.76554623C>T
CLNSRC
CLNACC	RCV000151469.1,