rs1060499962

Orientation

plus

Stabilized

plus

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

Make rs1060499962(-;-)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1222999

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs1060499962
dbSNP (classic)	rs1060499962
ClinGen	rs1060499962
ebi	rs1060499962
HLI	rs1060499962
Exac	rs1060499962
Gnomad	rs1060499962
Varsome	rs1060499962
LitVar	rs1060499962
Map	rs1060499962
PheGenI	rs1060499962
Biobank	rs1060499962
1000 genomes	rs1060499962
hgdp	rs1060499962
ensembl	rs1060499962
geneview	rs1060499962
scholar	rs1060499962
google	rs1060499962
pharmgkb	rs1060499962
gwascentral	rs1060499962
openSNP	rs1060499962
23andMe	rs1060499962
SNPshot	rs1060499962
SNPdbe	rs1060499962
MSV3d	rs1060499962
GWAS Ctlg	rs1060499962

Max Magnitude

5.8

ClinVar
Risk	rs1060499962(-;-)
Alt	rs1060499962(-;-)
Reference	Rs1060499962(AA;AA)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1222998_1222999delAA
CLNSRC
CLNACC	RCV000474608.1,