rs730881985

Merged into

rs587782424

Orientation

plus

Stabilized

plus

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

Make rs730881985(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1219351

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs730881985
dbSNP (classic)	rs730881985
ClinGen	rs730881985
ebi	rs730881985
HLI	rs730881985
Exac	rs730881985
Gnomad	rs730881985
Varsome	rs730881985
LitVar	rs730881985
Map	rs730881985
PheGenI	rs730881985
Biobank	rs730881985
1000 genomes	rs730881985
hgdp	rs730881985
ensembl	rs730881985
geneview	rs730881985
scholar	rs730881985
google	rs730881985
pharmgkb	rs730881985
gwascentral	rs730881985
openSNP	rs730881985
23andMe	rs730881985
SNPshot	rs730881985
SNPdbe	rs730881985
MSV3d	rs730881985
GWAS Ctlg	rs730881985

Status

Merged into rs587782424

Max Magnitude

5.8

ClinVar
Risk
Alt
Reference	Rs730881985(GT;GT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1219350_1219351delTG
CLNSRC
CLNACC	RCV000161008.2,