rs876658584

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 rs876658584(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

1218415

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs876658584
dbSNP (classic)	rs876658584
ClinGen	rs876658584
ebi	rs876658584
HLI	rs876658584
Exac	rs876658584
Gnomad	rs876658584
Varsome	rs876658584
LitVar	rs876658584
Map	rs876658584
PheGenI	rs876658584
Biobank	rs876658584
1000 genomes	rs876658584
hgdp	rs876658584
ensembl	rs876658584
geneview	rs876658584
scholar	rs876658584
google	rs876658584
pharmgkb	rs876658584
gwascentral	rs876658584
openSNP	rs876658584
23andMe	rs876658584
SNPshot	rs876658584
SNPdbe	rs876658584
MSV3d	rs876658584
GWAS Ctlg	rs876658584

Max Magnitude

5.8

ClinVar
Risk	rs876658584(G;G)
Alt	rs876658584(G;G)
Reference	Rs876658584(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1218414A>G
CLNSRC
CLNACC	RCV000222975.1,