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rs786204180

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204180(-;-)
Make rs786204180(-;AATC)
Make rs786204180(AATC;AATC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806628
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs786204180
ebirs786204180
HLIrs786204180
Exacrs786204180
Varsomers786204180
Maprs786204180
PheGenIrs786204180
hapmaprs786204180
1000 genomesrs786204180
hgdprs786204180
ensemblrs786204180
gopubmedrs786204180
geneviewrs786204180
scholarrs786204180
googlers786204180
pharmgkbrs786204180
gwascentralrs786204180
openSNPrs786204180
23andMers786204180
23andMe allrs786204180
SNP Nexus

SNPshotrs786204180
SNPdbers786204180
MSV3drs786204180
GWAS Ctlgrs786204180
Max Magnitude0
ClinVar
Risk rs786204180(AATC;AATC)
Alt rs786204180(AATC;AATC)
Reference rs786204180(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033769_48033772dupATCA
CLNSRC
CLNACC RCV000164350.1, RCV000168228.1, RCV000202005.1,