rs587776660

Orientation

plus

Stabilized

plus

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

Make rs587776660(-;-)

Reference

GRCh38 38.1/142

Chromosome

19

Position

1221994

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs587776660
dbSNP (classic)	rs587776660
ClinGen	rs587776660
ebi	rs587776660
HLI	rs587776660
Exac	rs587776660
Gnomad	rs587776660
Varsome	rs587776660
LitVar	rs587776660
Map	rs587776660
PheGenI	rs587776660
Biobank	rs587776660
1000 genomes	rs587776660
hgdp	rs587776660
ensembl	rs587776660
geneview	rs587776660
scholar	rs587776660
google	rs587776660
pharmgkb	rs587776660
gwascentral	rs587776660
openSNP	rs587776660
23andMe	rs587776660
SNPshot	rs587776660
SNPdbe	rs587776660
MSV3d	rs587776660
GWAS Ctlg	rs587776660

Max Magnitude

5.8

ClinVar
Risk	rs587776660(-;-)
Alt	rs587776660(-;-)
Reference	Rs587776660(TCCGGCAGC;TCCGGCAGC)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1221993_1222001delTCCGGCAGC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007872.4,