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rs2075789

From SNPedia

Orientationminus
Stabilizedminus
Make rs2075789(A;A)
Make rs2075789(A;G)
Make rs2075789(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31740551
GeneMSH5
is asnp
is mentioned by
dbSNPrs2075789
ebirs2075789
HLIrs2075789
Exacrs2075789
Varsomers2075789
Maprs2075789
PheGenIrs2075789
hapmaprs2075789
1000 genomesrs2075789
hgdprs2075789
ensemblrs2075789
gopubmedrs2075789
geneviewrs2075789
scholarrs2075789
googlers2075789
pharmgkbrs2075789
gwascentralrs2075789
openSNPrs2075789
23andMers2075789
23andMe allrs2075789
SNP Nexus

SNPshotrs2075789
SNPdbers2075789
MSV3drs2075789
GWAS Ctlgrs2075789
GMAF0.1212
Max Magnitude
? (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 17409188OA-icon.png] Role for Msh5 in the regulation of Ig class switch recombination.


GET Evidence
MSH5-P29S
aa_change Pro29Ser
aa_change_short P29S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0623594
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