rs121913324

Orientation

plus

Stabilized

plus

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

Make rs121913324(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1207022

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs121913324
dbSNP (classic)	rs121913324
ClinGen	rs121913324
ebi	rs121913324
HLI	rs121913324
Exac	rs121913324
Gnomad	rs121913324
Varsome	rs121913324
LitVar	rs121913324
Map	rs121913324
PheGenI	rs121913324
Biobank	rs121913324
1000 genomes	rs121913324
hgdp	rs121913324
ensembl	rs121913324
geneview	rs121913324
scholar	rs121913324
google	rs121913324
pharmgkb	rs121913324
gwascentral	rs121913324
openSNP	rs121913324
23andMe	rs121913324
SNPshot	rs121913324
SNPdbe	rs121913324
MSV3d	rs121913324
GWAS Ctlg	rs121913324

Max Magnitude

5.8

c.109C>T (p.Gln37Ter)

23andMe name: i6018839

ClinVar
Risk	rs121913324(T;T)
Alt	rs121913324(T;T)
Reference	Rs121913324(C;C)
Significance	Pathogenic
Disease	Neoplasm Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Neoplasm Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1207021C>T
CLNSRC
CLNACC	RCV000424203.1, RCV000492327.1,