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rs1800935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1800935(C;C)
Make rs1800935(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47795976
GeneMSH6
is asnp
is mentioned by
dbSNPrs1800935
ebirs1800935
HLIrs1800935
Exacrs1800935
Varsomers1800935
Maprs1800935
PheGenIrs1800935
hapmaprs1800935
1000 genomesrs1800935
hgdprs1800935
ensemblrs1800935
gopubmedrs1800935
geneviewrs1800935
scholarrs1800935
googlers1800935
pharmgkbrs1800935
gwascentralrs1800935
openSNPrs1800935
23andMers1800935
23andMe allrs1800935
SNP Nexus

SNPshotrs1800935
SNPdbers1800935
MSV3drs1800935
GWAS Ctlgrs1800935
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 24755277] Variations in mismatch repair genes and colorectal cancer risk and clinical outcome


ClinVar
Risk rs1800935(C;C)
Alt rs1800935(C;C)
Reference rs1800935(T;T)
Significance Non-pathogenic
Disease Lynch syndrome not specified Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48023115T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000030275.3, RCV000035326.7, RCV000131276.2,