rs587776658

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

Make rs587776658(A;A)

Reference

GRCh38 38.1/142

Chromosome

19

Position

1220372

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs587776658
dbSNP (classic)	rs587776658
ClinGen	rs587776658
ebi	rs587776658
HLI	rs587776658
Exac	rs587776658
Gnomad	rs587776658
Varsome	rs587776658
LitVar	rs587776658
Map	rs587776658
PheGenI	rs587776658
Biobank	rs587776658
1000 genomes	rs587776658
hgdp	rs587776658
ensembl	rs587776658
geneview	rs587776658
scholar	rs587776658
google	rs587776658
pharmgkb	rs587776658
gwascentral	rs587776658
openSNP	rs587776658
23andMe	rs587776658
SNPshot	rs587776658
SNPdbe	rs587776658
MSV3d	rs587776658
GWAS Ctlg	rs587776658

Max Magnitude

5.8

c.465-1G>A

23andMe name: i5006545

ClinVar
Risk	rs587776658(A;A)
Alt	rs587776658(A;A)
Reference	Rs587776658(G;G)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1220371G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007868.3,