rs786205864

Orientation

plus

Stabilized

plus

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

Make rs786205864(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

1221322

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs786205864
dbSNP (classic)	rs786205864
ClinGen	rs786205864
ebi	rs786205864
HLI	rs786205864
Exac	rs786205864
Gnomad	rs786205864
Varsome	rs786205864
LitVar	rs786205864
Map	rs786205864
PheGenI	rs786205864
Biobank	rs786205864
1000 genomes	rs786205864
hgdp	rs786205864
ensembl	rs786205864
geneview	rs786205864
scholar	rs786205864
google	rs786205864
pharmgkb	rs786205864
gwascentral	rs786205864
openSNP	rs786205864
23andMe	rs786205864
SNPshot	rs786205864
SNPdbe	rs786205864
MSV3d	rs786205864
GWAS Ctlg	rs786205864

Max Magnitude

5.8

ClinVar
Risk	rs786205864(C;C)
Alt	rs786205864(C;C)
Reference	Rs786205864(-;-)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1221321dupC
CLNSRC
CLNACC	RCV000172824.1,