rs730881977

Orientation

plus

Stabilized

plus

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

Make rs730881977(A;A)

Make rs730881977(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1221230

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs730881977
dbSNP (classic)	rs730881977
ClinGen	rs730881977
ebi	rs730881977
HLI	rs730881977
Exac	rs730881977
Gnomad	rs730881977
Varsome	rs730881977
LitVar	rs730881977
Map	rs730881977
PheGenI	rs730881977
Biobank	rs730881977
1000 genomes	rs730881977
hgdp	rs730881977
ensembl	rs730881977
geneview	rs730881977
scholar	rs730881977
google	rs730881977
pharmgkb	rs730881977
gwascentral	rs730881977
openSNP	rs730881977
23andMe	rs730881977
SNPshot	rs730881977
SNPdbe	rs730881977
MSV3d	rs730881977
GWAS Ctlg	rs730881977

Max Magnitude

5.8

ClinVar
Risk	rs730881977(A;A)
Alt	rs730881977(A;A)
Reference	Rs730881977(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1221229G>A
CLNSRC
CLNACC	RCV000160996.1,