rs727504171

Orientation

plus

Stabilized

plus

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

Make rs727504171(G;G)

Make rs727504171(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1221994

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs727504171
dbSNP (classic)	rs727504171
ClinGen	rs727504171
ebi	rs727504171
HLI	rs727504171
Exac	rs727504171
Gnomad	rs727504171
Varsome	rs727504171
LitVar	rs727504171
Map	rs727504171
PheGenI	rs727504171
Biobank	rs727504171
1000 genomes	rs727504171
hgdp	rs727504171
ensembl	rs727504171
geneview	rs727504171
scholar	rs727504171
google	rs727504171
pharmgkb	rs727504171
gwascentral	rs727504171
openSNP	rs727504171
23andMe	rs727504171
SNPshot	rs727504171
SNPdbe	rs727504171
MSV3d	rs727504171
GWAS Ctlg	rs727504171

Max Magnitude

5.8

ClinVar
Risk	rs727504171(G;G)
Alt	rs727504171(G;G)
Reference	Rs727504171(T;T)
Significance	Probable-Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1221993T>G
CLNSRC
CLNACC	RCV000153993.3,