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rs864622585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGTAA;GGTAA) 0 common in clinvar
Make rs864622585(GGTAA;T)
Make rs864622585(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800291
GeneMSH6
is asnp
is mentioned by
dbSNPrs864622585
dbSNP (old)rs864622585
ClinGenrs864622585
ebirs864622585
HLIrs864622585
Exacrs864622585
Varsomers864622585
Maprs864622585
PheGenIrs864622585
Biobankrs864622585
1000 genomesrs864622585
hgdprs864622585
ensemblrs864622585
gopubmedrs864622585
geneviewrs864622585
scholarrs864622585
googlers864622585
pharmgkbrs864622585
gwascentralrs864622585
openSNPrs864622585
23andMers864622585
23andMe allrs864622585
SNP Nexus

SNPshotrs864622585
SNPdbers864622585
MSV3drs864622585
GWAS Ctlgrs864622585
Max Magnitude0
ClinVar
Risk rs864622585(T;T)
Alt rs864622585(T;T)
Reference Rs864622585(GGTAA;GGTAA)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027430_48027434delGGTAAinsT
CLNSRC
CLNACC RCV000204888.1, RCV000218163.1,