rs137853078

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 rs137853078(A;A)

Reference

GRCh38 38.1/141

Chromosome

19

Position

1220396

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs137853078
dbSNP (classic)	rs137853078
ClinGen	rs137853078
ebi	rs137853078
HLI	rs137853078
Exac	rs137853078
Gnomad	rs137853078
Varsome	rs137853078
LitVar	rs137853078
Map	rs137853078
PheGenI	rs137853078
Biobank	rs137853078
1000 genomes	rs137853078
hgdp	rs137853078
ensembl	rs137853078
geneview	rs137853078
scholar	rs137853078
google	rs137853078
pharmgkb	rs137853078
gwascentral	rs137853078
openSNP	rs137853078
23andMe	rs137853078
SNPshot	rs137853078
SNPdbe	rs137853078
MSV3d	rs137853078
GWAS Ctlg	rs137853078

Max Magnitude

5.8

c.488G>A (p.Gly163Asp)

23andMe name: i5006536

OMIM	602216
Desc
Variant	0011
Related	also

ClinVar
Risk	rs137853078(A;A)
Alt	rs137853078(A;A)
Reference	Rs137853078(G;G)
Significance	Pathogenic
Disease	Malignant tumor of testis Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	Malignant tumor of testis Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1220395G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007874.6, RCV000492740.1,