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

rs786204320

From SNPedia

Orientationplus
Geno Mag Summary
(GGTTG;GGTTG) 0 common in clinvar
Make rs786204320(AAATTAAGA;AAATTAAGA)
Make rs786204320(AAATTAAGA;GGTTG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47414268
GeneMSH2
is asnp
is mentioned by
dbSNPrs786204320
ebirs786204320
HLIrs786204320
Exacrs786204320
Varsomers786204320
Maprs786204320
PheGenIrs786204320
hapmaprs786204320
1000 genomesrs786204320
hgdprs786204320
ensemblrs786204320
gopubmedrs786204320
geneviewrs786204320
scholarrs786204320
googlers786204320
pharmgkbrs786204320
gwascentralrs786204320
openSNPrs786204320
23andMers786204320
23andMe allrs786204320
SNP Nexus

SNPshotrs786204320
SNPdbers786204320
MSV3drs786204320
GWAS Ctlgrs786204320
Max Magnitude0
ClinVar
Risk rs786204320(AAATTAAGA;AAATTAAGA)
Alt rs786204320(AAATTAAGA;AAATTAAGA)
Reference rs786204320(GGTTG;GGTTG)
Significance Probable-Pathogenic
Disease Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47641407_47641411delinsAAATTAAGA
CLNSRC
CLNACC RCV000168726.1,