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rs786201855

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201855(-;-)
Make rs786201855(-;ATCA)
Make rs786201855(ATCA;ATCA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806633
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs786201855
ebirs786201855
HLIrs786201855
Exacrs786201855
Varsomers786201855
Maprs786201855
PheGenIrs786201855
hapmaprs786201855
1000 genomesrs786201855
hgdprs786201855
ensemblrs786201855
gopubmedrs786201855
geneviewrs786201855
scholarrs786201855
googlers786201855
pharmgkbrs786201855
gwascentralrs786201855
openSNPrs786201855
23andMers786201855
23andMe allrs786201855
SNP Nexus

SNPshotrs786201855
SNPdbers786201855
MSV3drs786201855
GWAS Ctlgrs786201855
Max Magnitude0
ClinVar
Risk rs786201855(AATC;AATC)
Alt rs786201855(AATC;AATC)
Reference rs786201855(;)
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,