rs730881979

Orientation

plus

Stabilized

plus

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

Make rs730881979(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1220434

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs730881979
dbSNP (classic)	rs730881979
ClinGen	rs730881979
ebi	rs730881979
HLI	rs730881979
Exac	rs730881979
Gnomad	rs730881979
Varsome	rs730881979
LitVar	rs730881979
Map	rs730881979
PheGenI	rs730881979
Biobank	rs730881979
1000 genomes	rs730881979
hgdp	rs730881979
ensembl	rs730881979
geneview	rs730881979
scholar	rs730881979
google	rs730881979
pharmgkb	rs730881979
gwascentral	rs730881979
openSNP	rs730881979
23andMe	rs730881979
SNPshot	rs730881979
SNPdbe	rs730881979
MSV3d	rs730881979
GWAS Ctlg	rs730881979

Max Magnitude

5.8

ClinVar
Risk	rs730881979(A;A)
Alt	rs730881979(A;A)
Reference	Rs730881979(G;G)
Significance	Probable-Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1220433G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000429467.1,