rs754896169

Orientation

plus

Stabilized

plus

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

Make rs754896169(C;T)

Make rs754896169(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

132129530

Gene

KCNQ3

is a	snp
is	mentioned by
dbSNP	rs754896169
dbSNP (classic)	rs754896169
ClinGen	rs754896169
ebi	rs754896169
HLI	rs754896169
Exac	rs754896169
Gnomad	rs754896169
Varsome	rs754896169
LitVar	rs754896169
Map	rs754896169
PheGenI	rs754896169
Biobank	rs754896169
1000 genomes	rs754896169
hgdp	rs754896169
ensembl	rs754896169
geneview	rs754896169
scholar	rs754896169
google	rs754896169
pharmgkb	rs754896169
gwascentral	rs754896169
openSNP	rs754896169
23andMe	rs754896169
SNPshot	rs754896169
SNPdbe	rs754896169
MSV3d	rs754896169
GWAS Ctlg	rs754896169

Max Magnitude

0

ClinVar
Risk	rs754896169(T;T)
Alt	rs754896169(T;T)
Reference	Rs754896169(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ3
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.133141777C>T
CLNSRC
CLNACC	RCV000187998.1,