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rs786204048

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs786204048(-;-)
Make rs786204048(-;AC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800127
GeneMSH6
is asnp
is mentioned by
dbSNPrs786204048
ebirs786204048
HLIrs786204048
Exacrs786204048
Varsomers786204048
Maprs786204048
PheGenIrs786204048
hapmaprs786204048
1000 genomesrs786204048
hgdprs786204048
ensemblrs786204048
gopubmedrs786204048
geneviewrs786204048
scholarrs786204048
googlers786204048
pharmgkbrs786204048
gwascentralrs786204048
openSNPrs786204048
23andMers786204048
23andMe allrs786204048
SNP Nexus

SNPshotrs786204048
SNPdbers786204048
MSV3drs786204048
GWAS Ctlgrs786204048
Max Magnitude0
ClinVar
Risk rs786204048(;)
Alt rs786204048(;)
Reference rs786204048(AC;AC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027266_48027267delAC
CLNSRC
CLNACC RCV000167893.1,