rs1057517830

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 rs1057517830(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1221212

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs1057517830
dbSNP (classic)	rs1057517830
ClinGen	rs1057517830
ebi	rs1057517830
HLI	rs1057517830
Exac	rs1057517830
Gnomad	rs1057517830
Varsome	rs1057517830
LitVar	rs1057517830
Map	rs1057517830
PheGenI	rs1057517830
Biobank	rs1057517830
1000 genomes	rs1057517830
hgdp	rs1057517830
ensembl	rs1057517830
geneview	rs1057517830
scholar	rs1057517830
google	rs1057517830
pharmgkb	rs1057517830
gwascentral	rs1057517830
openSNP	rs1057517830
23andMe	rs1057517830
SNPshot	rs1057517830
SNPdbe	rs1057517830
MSV3d	rs1057517830
GWAS Ctlg	rs1057517830

Max Magnitude

5.8

ClinVar
Risk	rs1057517830(A;A)
Alt	rs1057517830(A;A)
Reference	Rs1057517830(G;G)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	STK11
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000019.9:g.1221211G>A
CLNSRC
CLNACC	RCV000413399.1, RCV000492178.1,