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rs10849

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs10849(A;A)
Make rs10849(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position37053579
GeneLRRFIP2
is asnp
is mentioned by
dbSNPrs10849
dbSNP (old)rs10849
ClinGenrs10849
ebirs10849
HLIrs10849
Exacrs10849
Gnomadrs10849
Varsomers10849
Maprs10849
PheGenIrs10849
Biobankrs10849
1000 genomesrs10849
hgdprs10849
ensemblrs10849
gopubmedrs10849
geneviewrs10849
scholarrs10849
googlers10849
pharmgkbrs10849
gwascentralrs10849
openSNPrs10849
23andMers10849
23andMe allrs10849
SNPshotrs10849
SNPdbers10849
MSV3drs10849
GWAS Ctlgrs10849
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 28445130] Single nucleotide polymorphisms in MLH1 predict poor prognosis of hepatocellular carcinoma in a Chinese population.


ClinVar
Risk rs10849(A;A) rs10849(C;C)
Alt rs10849(A;A) rs10849(C;C)
Reference Rs10849(G;G)
Significance Non-pathogenic
Disease Lynch syndrome
Variation info
Gene LRRFIP2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000003.11:g.37095070C>T
CLNSRC
CLNACC RCV000075054.2,



[PMID 29108386] Single nucleotide polymorphisms in MLH1 predict poor prognosis of hepatocellular carcinoma in a Chinese population.