Rs1802127

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Orientationplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1802127(C;T)
Make rs1802127(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31762148
GeneC6orf26, MSH5
is asnp
is mentioned by
dbSNPrs1802127
Exacrs1802127
PheGenIrs1802127
nextbiors1802127
hapmaprs1802127
1000 genomesrs1802127
hgdprs1802127
ensemblrs1802127
gopubmedrs1802127
geneviewrs1802127
scholarrs1802127
googlers1802127
pharmgkbrs1802127
gwascentralrs1802127
openSNPrs1802127
23andMers1802127
23andMe allrs1802127
SNP Nexus

SNPshotrs1802127
SNPdbers1802127
MSV3drs1802127
Merged fromRs28399984
GMAF0.04959
? (C;C) (C;T) (T;T) 28
? (C;C) (C;T) (T;T)
[PMID 16741161OA-icon.png] Variants in the GH-IGF axis confer susceptibility to lung cancer.


[PMID 17409188OA-icon.png] Role for Msh5 in the regulation of Ig class switch recombination.


GET Evidence
MSH5-P787S
aa_change Pro787Ser
aa_change_short P787S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0556795
summary



[PMID 23238918] Genome-wide pathway analysis of a genome-wide association study on multiple sclerosis.