rs797044966

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CTC;CTC)	0	common in clinvar
(I;I)	0	common genotype

Make rs797044966(-;-)

Make rs797044966(-;CCT)

Make rs797044966(CCT;CCT)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

40819444

Gene

KCNQ4

is a	snp
is	mentioned by
dbSNP	rs797044966
dbSNP (classic)	rs797044966
ClinGen	rs797044966
ebi	rs797044966
HLI	rs797044966
Exac	rs797044966
Gnomad	rs797044966
Varsome	rs797044966
LitVar	rs797044966
Map	rs797044966
PheGenI	rs797044966
Biobank	rs797044966
1000 genomes	rs797044966
hgdp	rs797044966
ensembl	rs797044966
geneview	rs797044966
scholar	rs797044966
google	rs797044966
pharmgkb	rs797044966
gwascentral	rs797044966
openSNP	rs797044966
23andMe	rs797044966
SNPshot	rs797044966
SNPdbe	rs797044966
MSV3d	rs797044966
GWAS Ctlg	rs797044966

Max Magnitude

0

ClinVar
Risk	rs797044966(-;-)
Alt	rs797044966(-;-)
Reference	Rs797044966(CTC;CTC)
Significance	Pathogenic
Disease	DFNA 2 Nonsyndromic Hearing Loss not provided
Variation	info
Gene	KCNQ4
CLNDBN	DFNA 2 Nonsyndromic Hearing Loss not provided
Reversed	0
HGVS	NC_000001.10:g.41285116_41285118delCCT
CLNSRC
CLNACC	RCV000194270.1, RCV000484405.1,