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rs63749900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749900(C;C)
Make rs63749900(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37048596
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749900
ebirs63749900
HLIrs63749900
Exacrs63749900
Varsomers63749900
Maprs63749900
PheGenIrs63749900
hapmaprs63749900
1000 genomesrs63749900
hgdprs63749900
ensemblrs63749900
gopubmedrs63749900
geneviewrs63749900
scholarrs63749900
googlers63749900
pharmgkbrs63749900
gwascentralrs63749900
openSNPrs63749900
23andMers63749900
23andMe allrs63749900
SNP Nexus

SNPshotrs63749900
SNPdbers63749900
MSV3drs63749900
GWAS Ctlgrs63749900
Max Magnitude0
ClinVar
Risk rs63749900(A,C,T;A,C,T)
Alt rs63749900(A,C,T;A,C,T)
Reference rs63749900(G;G)
Significance Pathogenic
Disease Lynch syndrome not specified
Variation info
Gene MLH1
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37090087G>A; NC_000003.11:g.37090087G>C; NC_000003.11:g.37090087G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075446.3, RCV000121365.1, RCV000075447.2, RCV000075448.2,