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rs755583143

From SNPedia

Orientationplus
Geno Mag Summary
(TAAAA;TAAAA) 0 common in clinvar
Make rs755583143(-;-)
Make rs755583143(-;TAAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47414420
GeneMSH2
is asnp
is mentioned by
dbSNPrs755583143
ebirs755583143
HLIrs755583143
Exacrs755583143
Varsomers755583143
Maprs755583143
PheGenIrs755583143
hapmaprs755583143
1000 genomesrs755583143
hgdprs755583143
ensemblrs755583143
gopubmedrs755583143
geneviewrs755583143
scholarrs755583143
googlers755583143
pharmgkbrs755583143
gwascentralrs755583143
openSNPrs755583143
23andMers755583143
23andMe allrs755583143
SNP Nexus

SNPshotrs755583143
SNPdbers755583143
MSV3drs755583143
GWAS Ctlgrs755583143
Max Magnitude0
ClinVar
Risk rs755583143(;)
Alt rs755583143(;)
Reference rs755583143(TAAAA;TAAAA)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641559_47641563delTAAAA
CLNSRC
CLNACC RCV000227845.1,