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rs863224475

From SNPedia

Orientationplus
Make rs863224475(-;-)
Make rs863224475(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800072
GeneMSH6
is asnp
is mentioned by
dbSNPrs863224475
ebirs863224475
HLIrs863224475
Exacrs863224475
Varsomers863224475
Maprs863224475
PheGenIrs863224475
hapmaprs863224475
1000 genomesrs863224475
hgdprs863224475
ensemblrs863224475
gopubmedrs863224475
geneviewrs863224475
scholarrs863224475
googlers863224475
pharmgkbrs863224475
gwascentralrs863224475
openSNPrs863224475
23andMers863224475
23andMe allrs863224475
SNP Nexus

SNPshotrs863224475
SNPdbers863224475
MSV3drs863224475
GWAS Ctlgrs863224475
Max Magnitude
ClinVar
Risk rs863224475(;)
Alt rs863224475(;)
Reference rs863224475(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027211delG
CLNSRC
CLNACC RCV000197466.1,