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rs1059060

From SNPedia

Merged intors17420802
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1059060(A;G)
Make rs1059060(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position5977709
GenePMS2
is asnp
is mentioned by
dbSNPrs1059060
ebirs1059060
HLIrs1059060
Exacrs1059060
Varsomers1059060
Maprs1059060
PheGenIrs1059060
hapmaprs1059060
1000 genomesrs1059060
hgdprs1059060
ensemblrs1059060
gopubmedrs1059060
geneviewrs1059060
scholarrs1059060
googlers1059060
pharmgkbrs1059060
gwascentralrs1059060
openSNPrs1059060
23andMers1059060
23andMe allrs1059060
SNP Nexus

SNPshotrs1059060
SNPdbers1059060
MSV3drs1059060
GWAS Ctlgrs1059060
StatusMerged into rs17420802
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22594646OA-icon.png] Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility[PMID 17267408OA-icon.png] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.
GET Evidence
PMS2-N775S
aa_change Asn775Ser
aa_change_short N775S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.015873
summary



[PMID 26027715] Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China