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rs1800932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1800932(A;G)
Make rs1800932(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47790942
GeneMSH6
is asnp
is mentioned by
dbSNPrs1800932
ebirs1800932
HLIrs1800932
Exacrs1800932
Varsomers1800932
Maprs1800932
PheGenIrs1800932
hapmaprs1800932
1000 genomesrs1800932
hgdprs1800932
ensemblrs1800932
gopubmedrs1800932
geneviewrs1800932
scholarrs1800932
googlers1800932
pharmgkbrs1800932
gwascentralrs1800932
openSNPrs1800932
23andMers1800932
23andMe allrs1800932
SNP Nexus

SNPshotrs1800932
SNPdbers1800932
MSV3drs1800932
GWAS Ctlgrs1800932
GMAF0.1042
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 20149637] Common variants in human CRC genes as low-risk alleles


ClinVar
Risk rs1800932(G;G)
Alt rs1800932(G;G)
Reference rs1800932(A;A)
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.48018081A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000030265.3, RCV000035321.7, RCV000162362.1,



[PMID 20386703OA-icon.png] Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.


[PMID 10537275] Germ-line msh6 mutations in colorectal cancer families.


[PMID 15805151OA-icon.png] No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer.


[PMID 24357391OA-icon.png] DNA mismatch repair gene MSH6 implicated in determining age at natural menopause