rs1060499961

Orientation

plus

Stabilized

plus

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

Make rs1060499961(-;-)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1207042

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs1060499961
dbSNP (classic)	rs1060499961
ClinGen	rs1060499961
ebi	rs1060499961
HLI	rs1060499961
Exac	rs1060499961
Gnomad	rs1060499961
Varsome	rs1060499961
LitVar	rs1060499961
Map	rs1060499961
PheGenI	rs1060499961
Biobank	rs1060499961
1000 genomes	rs1060499961
hgdp	rs1060499961
ensembl	rs1060499961
geneview	rs1060499961
scholar	rs1060499961
google	rs1060499961
pharmgkb	rs1060499961
gwascentral	rs1060499961
openSNP	rs1060499961
23andMe	rs1060499961
SNPshot	rs1060499961
SNPdbe	rs1060499961
MSV3d	rs1060499961
GWAS Ctlg	rs1060499961

Max Magnitude

5.8

ClinVar
Risk	rs1060499961(-;-)
Alt	rs1060499961(-;-)
Reference	Rs1060499961(C;C)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1207041delC
CLNSRC
CLNACC	RCV000466541.1,