rs727504635

Orientation

plus

Stabilized

plus

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

Make rs727504635(-;-)

Make rs727504635(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

40818217

Gene

KCNQ4

is a	snp
is	mentioned by
dbSNP	rs727504635
dbSNP (classic)	rs727504635
ClinGen	rs727504635
ebi	rs727504635
HLI	rs727504635
Exac	rs727504635
Gnomad	rs727504635
Varsome	rs727504635
LitVar	rs727504635
Map	rs727504635
PheGenI	rs727504635
Biobank	rs727504635
1000 genomes	rs727504635
hgdp	rs727504635
ensembl	rs727504635
geneview	rs727504635
scholar	rs727504635
google	rs727504635
pharmgkb	rs727504635
gwascentral	rs727504635
openSNP	rs727504635
23andMe	rs727504635
SNPshot	rs727504635
SNPdbe	rs727504635
MSV3d	rs727504635
GWAS Ctlg	rs727504635

Max Magnitude

0

ClinVar
Risk	rs727504635(-;-)
Alt	rs727504635(-;-)
Reference	Rs727504635(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	KCNQ4
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000001.10:g.41283889delC
CLNSRC
CLNACC	RCV000155896.1,