rs886037859

Orientation

plus

Stabilized

plus

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

Make rs886037859(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

1220450

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs886037859
dbSNP (classic)	rs886037859
ClinGen	rs886037859
ebi	rs886037859
HLI	rs886037859
Exac	rs886037859
Gnomad	rs886037859
Varsome	rs886037859
LitVar	rs886037859
Map	rs886037859
PheGenI	rs886037859
Biobank	rs886037859
1000 genomes	rs886037859
hgdp	rs886037859
ensembl	rs886037859
geneview	rs886037859
scholar	rs886037859
google	rs886037859
pharmgkb	rs886037859
gwascentral	rs886037859
openSNP	rs886037859
23andMe	rs886037859
SNPshot	rs886037859
SNPdbe	rs886037859
MSV3d	rs886037859
GWAS Ctlg	rs886037859

Max Magnitude

5.8

ClinVar
Risk	rs886037859(G;G)
Alt	rs886037859(G;G)
Reference	Rs886037859(A;A)
Significance	Probable-Pathogenic
Disease	Peutz-Jeghers syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1220449A>G
CLNSRC
CLNACC	RCV000241351.1, RCV000492112.1,