rs886037926

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs886037926(A;G)

Make rs886037926(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

1220449

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs886037926
dbSNP (classic)	rs886037926
ClinGen	rs886037926
ebi	rs886037926
HLI	rs886037926
Exac	rs886037926
Gnomad	rs886037926
Varsome	rs886037926
LitVar	rs886037926
Map	rs886037926
PheGenI	rs886037926
Biobank	rs886037926
1000 genomes	rs886037926
hgdp	rs886037926
ensembl	rs886037926
geneview	rs886037926
scholar	rs886037926
google	rs886037926
pharmgkb	rs886037926
gwascentral	rs886037926
openSNP	rs886037926
23andMe	rs886037926
SNPshot	rs886037926
SNPdbe	rs886037926
MSV3d	rs886037926
GWAS Ctlg	rs886037926

Max Magnitude

0

ClinVar
Risk	rs886037926(G;G)
Alt	rs886037926(G;G)
Reference	Rs886037926(A;A)
Significance	Probable-Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1220448A>G
CLNSRC
CLNACC	RCV000240843.1,