rs1064796831

Orientation

plus

Stabilized

plus

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

Chromosome

19

Position

1221319

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs1064796831
dbSNP (classic)	rs1064796831
ClinGen	rs1064796831
ebi	rs1064796831
HLI	rs1064796831
Exac	rs1064796831
Gnomad	rs1064796831
Varsome	rs1064796831
LitVar	rs1064796831
Map	rs1064796831
PheGenI	rs1064796831
Biobank	rs1064796831
1000 genomes	rs1064796831
hgdp	rs1064796831
ensembl	rs1064796831
geneview	rs1064796831
scholar	rs1064796831
google	rs1064796831
pharmgkb	rs1064796831
gwascentral	rs1064796831
openSNP	rs1064796831
23andMe	rs1064796831
SNPshot	rs1064796831
SNPdbe	rs1064796831
MSV3d	rs1064796831
GWAS Ctlg	rs1064796831

Max Magnitude

5.8

ClinVar
Risk	rs1064796831(-;-)
Alt	rs1064796831(-;-)
Reference	Rs1064796831(CC;CC)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	STK11
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000019.9:g.1221318_1221319delCC
CLNSRC
CLNACC	RCV000221464.1, RCV000485596.1,