rs727504172

Orientation

plus

Stabilized

plus

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

Make rs727504172(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

1222983

Gene

STK11

is a	snp
is	mentioned by
dbSNP	rs727504172
dbSNP (classic)	rs727504172
ClinGen	rs727504172
ebi	rs727504172
HLI	rs727504172
Exac	rs727504172
Gnomad	rs727504172
Varsome	rs727504172
LitVar	rs727504172
Map	rs727504172
PheGenI	rs727504172
Biobank	rs727504172
1000 genomes	rs727504172
hgdp	rs727504172
ensembl	rs727504172
geneview	rs727504172
scholar	rs727504172
google	rs727504172
pharmgkb	rs727504172
gwascentral	rs727504172
openSNP	rs727504172
23andMe	rs727504172
SNPshot	rs727504172
SNPdbe	rs727504172
MSV3d	rs727504172
GWAS Ctlg	rs727504172

Max Magnitude

5.8

ClinVar
Risk	rs727504172(T;T)
Alt	rs727504172(T;T)
Reference	Rs727504172(A;A)
Significance	Pathogenic
Disease	Peutz-Jeghers syndrome
Variation	info
Gene	STK11
CLNDBN	Peutz-Jeghers syndrome
Reversed	0
HGVS	NC_000019.9:g.1222982A>T
CLNSRC	HGMD
CLNACC	RCV000153994.3,