rs587781856

Orientation

plus

Stabilized

plus

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

Make rs587781856(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1220482

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs587781856
dbSNP (classic)	rs587781856
ClinGen	rs587781856
ebi	rs587781856
HLI	rs587781856
Exac	rs587781856
Gnomad	rs587781856
Varsome	rs587781856
LitVar	rs587781856
Map	rs587781856
PheGenI	rs587781856
Biobank	rs587781856
1000 genomes	rs587781856
hgdp	rs587781856
ensembl	rs587781856
geneview	rs587781856
scholar	rs587781856
google	rs587781856
pharmgkb	rs587781856
gwascentral	rs587781856
openSNP	rs587781856
23andMe	rs587781856
SNPshot	rs587781856
SNPdbe	rs587781856
MSV3d	rs587781856
GWAS Ctlg	rs587781856

Max Magnitude

5.8

ClinVar
Risk	rs587781856(-;-)
Alt	rs587781856(-;-)
Reference	Rs587781856(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.1220481delA
CLNSRC
CLNACC	RCV000130164.2,