rs1057524439

Orientation

plus

Stabilized

plus

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

Make rs1057524439(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1221955

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs1057524439
dbSNP (classic)	rs1057524439
ClinGen	rs1057524439
ebi	rs1057524439
HLI	rs1057524439
Exac	rs1057524439
Gnomad	rs1057524439
Varsome	rs1057524439
LitVar	rs1057524439
Map	rs1057524439
PheGenI	rs1057524439
Biobank	rs1057524439
1000 genomes	rs1057524439
hgdp	rs1057524439
ensembl	rs1057524439
geneview	rs1057524439
scholar	rs1057524439
google	rs1057524439
pharmgkb	rs1057524439
gwascentral	rs1057524439
openSNP	rs1057524439
23andMe	rs1057524439
SNPshot	rs1057524439
SNPdbe	rs1057524439
MSV3d	rs1057524439
GWAS Ctlg	rs1057524439

Max Magnitude

5.8

ClinVar
Risk	rs1057524439(C;C)
Alt	rs1057524439(C;C)
Reference	Rs1057524439(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	STK11
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.1221954T>C
CLNSRC
CLNACC	RCV000434265.1,