rs587776661

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587776661(-;-)

Make rs587776661(-;G)

Reference

GRCh38 38.1/142

Chromosome

19

Position

1221977

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs587776661
dbSNP (classic)	rs587776661
ClinGen	rs587776661
ebi	rs587776661
HLI	rs587776661
Exac	rs587776661
Gnomad	rs587776661
Varsome	rs587776661
LitVar	rs587776661
Map	rs587776661
PheGenI	rs587776661
Biobank	rs587776661
1000 genomes	rs587776661
hgdp	rs587776661
ensembl	rs587776661
geneview	rs587776661
scholar	rs587776661
google	rs587776661
pharmgkb	rs587776661
gwascentral	rs587776661
openSNP	rs587776661
23andMe	rs587776661
SNPshot	rs587776661
SNPdbe	rs587776661
MSV3d	rs587776661
GWAS Ctlg	rs587776661

Max Magnitude

0

ClinVar
Risk	rs587776661(-;-)
Alt	rs587776661(-;-)
Reference	Rs587776661(G;G)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1221976delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007885.4,