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rs1057520009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520009(A;A)
Make rs1057520009(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position61492337
GeneXPO1
is asnp
is mentioned by
dbSNPrs1057520009
dbSNP (classic)rs1057520009
ClinGenrs1057520009
ebirs1057520009
HLIrs1057520009
Exacrs1057520009
Gnomadrs1057520009
Varsomers1057520009
LitVarrs1057520009
Maprs1057520009
PheGenIrs1057520009
Biobankrs1057520009
1000 genomesrs1057520009
hgdprs1057520009
ensemblrs1057520009
geneviewrs1057520009
scholarrs1057520009
googlers1057520009
pharmgkbrs1057520009
gwascentralrs1057520009
openSNPrs1057520009
23andMers1057520009
SNPshotrs1057520009
SNPdbers1057520009
MSV3drs1057520009
GWAS Ctlgrs1057520009
Max Magnitude0
ClinVar
Risk rs1057520009(A;A)
Alt rs1057520009(A;A)
Reference Rs1057520009(G;G)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms Adenocarcinoma of prostate Malignant neoplasm of body of uterus Neoplasm of breast Chronic lymphocytic leukemia
Variation info
Gene XPO1
CLNDBN Colorectal Neoplasms Adenocarcinoma of prostate Malignant neoplasm of body of uterus Neoplasm of breast Chronic lymphocytic leukemia
Reversed 1
HGVS NC_000002.11:g.61719472C>T
CLNSRC
CLNACC RCV000424120.1, RCV000433995.1, RCV000434826.1, RCV000442355.1, RCV000444890.1,