rs143167166

Orientation

plus

Stabilized

plus

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

Make rs143167166(A;A)

Make rs143167166(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150945375

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs143167166
dbSNP (classic)	rs143167166
ClinGen	rs143167166
ebi	rs143167166
HLI	rs143167166
Exac	rs143167166
Gnomad	rs143167166
Varsome	rs143167166
LitVar	rs143167166
Map	rs143167166
PheGenI	rs143167166
Biobank	rs143167166
1000 genomes	rs143167166
hgdp	rs143167166
ensembl	rs143167166
geneview	rs143167166
scholar	rs143167166
google	rs143167166
pharmgkb	rs143167166
gwascentral	rs143167166
openSNP	rs143167166
23andMe	rs143167166
SNPshot	rs143167166
SNPdbe	rs143167166
MSV3d	rs143167166
GWAS Ctlg	rs143167166

Max Magnitude

0

ClinVar
Risk	rs143167166(A;A)
Alt	rs143167166(A;A)
Reference	Rs143167166(G;G)
Significance	Untested
Disease	SUDDEN INFANT DEATH SYNDROME not specified
Variation	info
Gene	KCNH2
CLNDBN	SUDDEN INFANT DEATH SYNDROME not specified
Reversed	0
HGVS	NC_000007.13:g.150642463G>A
CLNSRC	ClinVar
CLNACC	RCV000058228.3, RCV000181918.2,