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rs175080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs175080(A;A)
Make rs175080(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position75047125
GeneMLH3
is asnp
is mentioned by
dbSNPrs175080
dbSNP (old)rs175080
ClinGenrs175080
ebirs175080
HLIrs175080
Exacrs175080
Gnomadrs175080
Varsomers175080
Maprs175080
PheGenIrs175080
Biobankrs175080
1000 genomesrs175080
hgdprs175080
ensemblrs175080
gopubmedrs175080
geneviewrs175080
scholarrs175080
googlers175080
pharmgkbrs175080
gwascentralrs175080
openSNPrs175080
23andMers175080
23andMe allrs175080
SNP Nexus

SNPshotrs175080
SNPdbers175080
MSV3drs175080
GWAS Ctlgrs175080
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 26027715] Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China


ClinVar
Risk rs175080(A;A)
Alt rs175080(A;A)
Reference Rs175080(G;G)
Significance Probable-non-pathogenic
Disease not specified Lynch syndrome
Variation info
Gene MLH3
CLNDBN not specified Lynch syndrome
Reversed 0
HGVS NC_000014.8:g.75513828G>A
CLNSRC
CLNACC RCV000253289.1, RCV000385582.1,