rs587776659

Orientation

plus

Stabilized

plus

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

Make rs587776659(-;-)

Reference

GRCh38 38.1/142

Chromosome

19

Position

1221312

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs587776659
dbSNP (classic)	rs587776659
ClinGen	rs587776659
ebi	rs587776659
HLI	rs587776659
Exac	rs587776659
Gnomad	rs587776659
Varsome	rs587776659
LitVar	rs587776659
Map	rs587776659
PheGenI	rs587776659
Biobank	rs587776659
1000 genomes	rs587776659
hgdp	rs587776659
ensembl	rs587776659
geneview	rs587776659
scholar	rs587776659
google	rs587776659
pharmgkb	rs587776659
gwascentral	rs587776659
openSNP	rs587776659
23andMe	rs587776659
SNPshot	rs587776659
SNPdbe	rs587776659
MSV3d	rs587776659
GWAS Ctlg	rs587776659

Max Magnitude

5.8

ClinVar
Risk	rs587776659(-;-)
Alt	rs587776659(-;-)
Reference	Rs587776659(TG;TG)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1221311_1221312delTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007870.3,