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rs63750448

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750448(A;C)
Make rs63750448(C;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position44351792
GeneGRN
is asnp
is mentioned by
dbSNPrs63750448
ebirs63750448
HLIrs63750448
Exacrs63750448
Varsomers63750448
Maprs63750448
PheGenIrs63750448
hapmaprs63750448
1000 genomesrs63750448
hgdprs63750448
ensemblrs63750448
gopubmedrs63750448
geneviewrs63750448
scholarrs63750448
googlers63750448
pharmgkbrs63750448
gwascentralrs63750448
openSNPrs63750448
23andMers63750448
23andMe allrs63750448
SNP Nexus

SNPshotrs63750448
SNPdbers63750448
MSV3drs63750448
GWAS Ctlgrs63750448
Max Magnitude0

[PMID 25986311] Association between MutL homolog 1 polymorphisms and the risk of colorectal cancer: a meta-analysis


ClinVar
Risk rs63750448(C;C)
Alt rs63750448(C;C)
Reference rs63750448(A;A)
Significance Untested
Disease not provided
Variation info
Gene GRN
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.42429160A>C
CLNSRC
CLNACC RCV000084475.1,