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rs786203350

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203350(-;-)
Make rs786203350(-;AT)
Make rs786203350(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47429790
GeneMSH2
is asnp
is mentioned by
dbSNPrs786203350
ebirs786203350
HLIrs786203350
Exacrs786203350
Varsomers786203350
Maprs786203350
PheGenIrs786203350
hapmaprs786203350
1000 genomesrs786203350
hgdprs786203350
ensemblrs786203350
gopubmedrs786203350
geneviewrs786203350
scholarrs786203350
googlers786203350
pharmgkbrs786203350
gwascentralrs786203350
openSNPrs786203350
23andMers786203350
23andMe allrs786203350
SNP Nexus

SNPshotrs786203350
SNPdbers786203350
MSV3drs786203350
GWAS Ctlgrs786203350
Max Magnitude0
ClinVar
Risk rs786203350(TA;TA)
Alt rs786203350(TA;TA)
Reference rs786203350(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47656929_47656930insAT
CLNSRC
CLNACC RCV000166624.1,