rs398123405

Orientation

plus

Stabilized

plus

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

Make rs398123405(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

1221963

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs398123405
dbSNP (classic)	rs398123405
ClinGen	rs398123405
ebi	rs398123405
HLI	rs398123405
Exac	rs398123405
Gnomad	rs398123405
Varsome	rs398123405
LitVar	rs398123405
Map	rs398123405
PheGenI	rs398123405
Biobank	rs398123405
1000 genomes	rs398123405
hgdp	rs398123405
ensembl	rs398123405
geneview	rs398123405
scholar	rs398123405
google	rs398123405
pharmgkb	rs398123405
gwascentral	rs398123405
openSNP	rs398123405
23andMe	rs398123405
SNPshot	rs398123405
SNPdbe	rs398123405
MSV3d	rs398123405
GWAS Ctlg	rs398123405

Max Magnitude

5.8

ClinVar
Risk	rs398123405(A;A) rs398123405(T;T)
Alt	rs398123405(A;A) rs398123405(T;T)
Reference	Rs398123405(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Hereditary cancer-predisposing syndrome Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1221962G>A; NC_000019.9:g.1221962G>T
CLNSRC	Ambry Genetics ClinVar Emory University
CLNACC	RCV000131978.2, RCV000078913.4,