rs199472811

Orientation

plus

Stabilized

plus

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

Make rs199472811(A;A)

Make rs199472811(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2777993

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472811
dbSNP (classic)	rs199472811
ClinGen	rs199472811
ebi	rs199472811
HLI	rs199472811
Exac	rs199472811
Gnomad	rs199472811
Varsome	rs199472811
LitVar	rs199472811
Map	rs199472811
PheGenI	rs199472811
Biobank	rs199472811
1000 genomes	rs199472811
hgdp	rs199472811
ensembl	rs199472811
geneview	rs199472811
scholar	rs199472811
google	rs199472811
pharmgkb	rs199472811
gwascentral	rs199472811
openSNP	rs199472811
23andMe	rs199472811
SNPshot	rs199472811
SNPdbe	rs199472811
MSV3d	rs199472811
GWAS Ctlg	rs199472811

Max Magnitude

0

ClinVar
Risk	rs199472811(A;A)
Alt	rs199472811(A;A)
Reference	Rs199472811(G;G)
Significance	Untested
Disease	SUDDEN INFANT DEATH SYNDROME
Variation	info
Gene	KCNQ1
CLNDBN	SUDDEN INFANT DEATH SYNDROME
Reversed	0
HGVS	NC_000011.9:g.2799223G>A
CLNSRC	ClinVar
CLNACC	RCV000057630.3,