rs772135867

Orientation

plus

Stabilized

plus

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

Make rs772135867(C;T)

Make rs772135867(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

40838474

Gene

KCNQ4

is a	snp
is	mentioned by
dbSNP	rs772135867
dbSNP (classic)	rs772135867
ClinGen	rs772135867
ebi	rs772135867
HLI	rs772135867
Exac	rs772135867
Gnomad	rs772135867
Varsome	rs772135867
LitVar	rs772135867
Map	rs772135867
PheGenI	rs772135867
Biobank	rs772135867
1000 genomes	rs772135867
hgdp	rs772135867
ensembl	rs772135867
geneview	rs772135867
scholar	rs772135867
google	rs772135867
pharmgkb	rs772135867
gwascentral	rs772135867
openSNP	rs772135867
23andMe	rs772135867
SNPshot	rs772135867
SNPdbe	rs772135867
MSV3d	rs772135867
GWAS Ctlg	rs772135867

Max Magnitude

0

ClinVar
Risk	rs772135867(T;T)
Alt	rs772135867(T;T)
Reference	Rs772135867(C;C)
Significance	Pathogenic
Disease	DFNA 2 Nonsyndromic Hearing Loss
Variation	info
Gene	KCNQ4
CLNDBN	DFNA 2 Nonsyndromic Hearing Loss
Reversed	0
HGVS	NC_000001.10:g.41304146C>T
CLNSRC
CLNACC	RCV000192858.1,