rs886044309

Orientation

plus

Stabilized

plus

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

Chromosome

8

Position

101599152

Gene

GRHL2

is a	snp
is	mentioned by
dbSNP	rs886044309
dbSNP (classic)	rs886044309
ClinGen	rs886044309
ebi	rs886044309
HLI	rs886044309
Exac	rs886044309
Gnomad	rs886044309
Varsome	rs886044309
LitVar	rs886044309
Map	rs886044309
PheGenI	rs886044309
Biobank	rs886044309
1000 genomes	rs886044309
hgdp	rs886044309
ensembl	rs886044309
geneview	rs886044309
scholar	rs886044309
google	rs886044309
pharmgkb	rs886044309
gwascentral	rs886044309
openSNP	rs886044309
23andMe	rs886044309
SNPshot	rs886044309
SNPdbe	rs886044309
MSV3d	rs886044309
GWAS Ctlg	rs886044309

Max Magnitude

0

ClinVar
Risk	rs886044309(A;A)
Alt	rs886044309(A;A)
Reference	Rs886044309(G;G)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	GRHL2
CLNDBN	Deafness, autosomal dominant 28
Reversed	0
HGVS	NC_000008.10:g.102611380G>A
CLNSRC
CLNACC	RCV000358123.1,