rs1057520606

Orientation

plus

Stabilized

plus

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

Make rs1057520606(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1221244

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs1057520606
dbSNP (classic)	rs1057520606
ClinGen	rs1057520606
ebi	rs1057520606
HLI	rs1057520606
Exac	rs1057520606
Gnomad	rs1057520606
Varsome	rs1057520606
LitVar	rs1057520606
Map	rs1057520606
PheGenI	rs1057520606
Biobank	rs1057520606
1000 genomes	rs1057520606
hgdp	rs1057520606
ensembl	rs1057520606
geneview	rs1057520606
scholar	rs1057520606
google	rs1057520606
pharmgkb	rs1057520606
gwascentral	rs1057520606
openSNP	rs1057520606
23andMe	rs1057520606
SNPshot	rs1057520606
SNPdbe	rs1057520606
MSV3d	rs1057520606
GWAS Ctlg	rs1057520606

Max Magnitude

5.8

ClinVar
Risk	rs1057520606(T;T)
Alt	rs1057520606(T;T)
Reference	Rs1057520606(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	STK11
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.1221243G>T
CLNSRC
CLNACC	RCV000423599.1,