rs727504567

Orientation

plus

Stabilized

plus

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

Make rs727504567(C;T)

Make rs727504567(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

75828590

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs727504567
dbSNP (classic)	rs727504567
ClinGen	rs727504567
ebi	rs727504567
HLI	rs727504567
Exac	rs727504567
Gnomad	rs727504567
Varsome	rs727504567
LitVar	rs727504567
Map	rs727504567
PheGenI	rs727504567
Biobank	rs727504567
1000 genomes	rs727504567
hgdp	rs727504567
ensembl	rs727504567
geneview	rs727504567
scholar	rs727504567
google	rs727504567
pharmgkb	rs727504567
gwascentral	rs727504567
openSNP	rs727504567
23andMe	rs727504567
SNPshot	rs727504567
SNPdbe	rs727504567
MSV3d	rs727504567
GWAS Ctlg	rs727504567

Max Magnitude

0

ClinVar
Risk	rs727504567(T;T)
Alt	rs727504567(T;T)
Reference	Rs727504567(C;C)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness not provided
Variation	info
Gene	MYO6
CLNDBN	Nonsyndromic hearing loss and deafness not provided
Reversed	0
HGVS	NC_000006.11:g.76538307C>T
CLNSRC
CLNACC	RCV000155733.1, RCV000480356.1,