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rs876658848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTGACATTAA;AGTGACATTAA) 0 common in clinvar
Make rs876658848(-;-)
Make rs876658848(-;GTGACATTAAA)
Make rs876658848(GTGACATTAAA;GTGACATTAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800195
GeneMSH6
is asnp
is mentioned by
dbSNPrs876658848
dbSNP (old)rs876658848
ClinGenrs876658848
ebirs876658848
HLIrs876658848
Exacrs876658848
Gnomadrs876658848
Varsomers876658848
Maprs876658848
PheGenIrs876658848
Biobankrs876658848
1000 genomesrs876658848
hgdprs876658848
ensemblrs876658848
gopubmedrs876658848
geneviewrs876658848
scholarrs876658848
googlers876658848
pharmgkbrs876658848
gwascentralrs876658848
openSNPrs876658848
23andMers876658848
23andMe allrs876658848
SNP Nexus

SNPshotrs876658848
SNPdbers876658848
MSV3drs876658848
GWAS Ctlgrs876658848
Max Magnitude0
ClinVar
Risk rs876658848(-;-)
Alt rs876658848(-;-)
Reference Rs876658848(AGTGACATTAA;AGTGACATTAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027334_48027344delGTGACATTAAA
CLNSRC
CLNACC RCV000219217.1,