rs730881973

Orientation

plus

Stabilized

plus

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

Make rs730881973(A;A)

Make rs730881973(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1220451

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs730881973
dbSNP (classic)	rs730881973
ClinGen	rs730881973
ebi	rs730881973
HLI	rs730881973
Exac	rs730881973
Gnomad	rs730881973
Varsome	rs730881973
LitVar	rs730881973
Map	rs730881973
PheGenI	rs730881973
Biobank	rs730881973
1000 genomes	rs730881973
hgdp	rs730881973
ensembl	rs730881973
geneview	rs730881973
scholar	rs730881973
google	rs730881973
pharmgkb	rs730881973
gwascentral	rs730881973
openSNP	rs730881973
23andMe	rs730881973
SNPshot	rs730881973
SNPdbe	rs730881973
MSV3d	rs730881973
GWAS Ctlg	rs730881973

Max Magnitude

5.8

ClinVar
Risk	rs730881973(A;A)
Alt	rs730881973(A;A)
Reference	Rs730881973(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1220450C>G
CLNSRC
CLNACC	RCV000492674.1,