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rs63751219

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63751219(-;-)
Make rs63751219(-;TA)
Make rs63751219(TA;TA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429793
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751219
ebirs63751219
HLIrs63751219
Exacrs63751219
Varsomers63751219
Maprs63751219
PheGenIrs63751219
hapmaprs63751219
1000 genomesrs63751219
hgdprs63751219
ensemblrs63751219
gopubmedrs63751219
geneviewrs63751219
scholarrs63751219
googlers63751219
pharmgkbrs63751219
gwascentralrs63751219
openSNPrs63751219
23andMers63751219
23andMe allrs63751219
SNP Nexus

SNPshotrs63751219
SNPdbers63751219
MSV3drs63751219
GWAS Ctlgrs63751219
Max Magnitude0
ClinVar
Risk rs63751219(TA;TA)
Alt rs63751219(TA;TA)
Reference rs63751219(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656931_47656932dupTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076044.2,