rs864622488

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	5.8	STK11 gene mutation associated with Peutz-Jeghers syndrome
(G;G)	0	common in clinvar
(G;T)	5.8	STK11 gene mutation associated with Peutz-Jeghers syndrome

Make rs864622488(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

1222987

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs864622488
dbSNP (classic)	rs864622488
ClinGen	rs864622488
ebi	rs864622488
HLI	rs864622488
Exac	rs864622488
Gnomad	rs864622488
Varsome	rs864622488
LitVar	rs864622488
Map	rs864622488
PheGenI	rs864622488
Biobank	rs864622488
1000 genomes	rs864622488
hgdp	rs864622488
ensembl	rs864622488
geneview	rs864622488
scholar	rs864622488
google	rs864622488
pharmgkb	rs864622488
gwascentral	rs864622488
openSNP	rs864622488
23andMe	rs864622488
SNPshot	rs864622488
SNPdbe	rs864622488
MSV3d	rs864622488
GWAS Ctlg	rs864622488

Max Magnitude

5.8

ClinVar
Risk	rs864622488(T;T)
Alt	rs864622488(T;T)
Reference	Rs864622488(G;G)
Significance	Probable-Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1222986G>T
CLNSRC
CLNACC	RCV000205568.1,