rs869320674

Orientation

minus

Stabilized

minus

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

Make rs869320674(-;-)

Make rs869320674(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

114403335

Gene

WHRN

is a	snp
is	mentioned by
dbSNP	rs869320674
dbSNP (classic)	rs869320674
ClinGen	rs869320674
ebi	rs869320674
HLI	rs869320674
Exac	rs869320674
Gnomad	rs869320674
Varsome	rs869320674
LitVar	rs869320674
Map	rs869320674
PheGenI	rs869320674
Biobank	rs869320674
1000 genomes	rs869320674
hgdp	rs869320674
ensembl	rs869320674
geneview	rs869320674
scholar	rs869320674
google	rs869320674
pharmgkb	rs869320674
gwascentral	rs869320674
openSNP	rs869320674
23andMe	rs869320674
SNPshot	rs869320674
SNPdbe	rs869320674
MSV3d	rs869320674
GWAS Ctlg	rs869320674

Max Magnitude

0

ClinVar
Risk	rs869320674(-;-)
Alt	rs869320674(-;-)
Reference	Rs869320674(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	WHRN DFNB31
CLNDBN	Deafness, autosomal recessive 31
Reversed	1
HGVS	NC_000009.11:g.117165615delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190401.2,