Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs63751700(-;-)
Make rs63751700(-;AT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475261
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751700
ebirs63751700
HLIrs63751700
Exacrs63751700
Varsomers63751700
Maprs63751700
PheGenIrs63751700
hapmaprs63751700
1000 genomesrs63751700
hgdprs63751700
ensemblrs63751700
gopubmedrs63751700
geneviewrs63751700
scholarrs63751700
googlers63751700
pharmgkbrs63751700
gwascentralrs63751700
openSNPrs63751700
23andMers63751700
23andMe allrs63751700
SNP Nexus

SNPshotrs63751700
SNPdbers63751700
MSV3drs63751700
GWAS Ctlgrs63751700
Max Magnitude0
ClinVar
Risk rs63751700(;)
Alt rs63751700(;)
Reference rs63751700(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702400_47702401delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076333.2,