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rs863224476

From SNPedia

Orientationplus
Make rs863224476(-;-)
Make rs863224476(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47803682
GeneMSH6
is asnp
is mentioned by
dbSNPrs863224476
ebirs863224476
HLIrs863224476
Exacrs863224476
Varsomers863224476
Maprs863224476
PheGenIrs863224476
hapmaprs863224476
1000 genomesrs863224476
hgdprs863224476
ensemblrs863224476
gopubmedrs863224476
geneviewrs863224476
scholarrs863224476
googlers863224476
pharmgkbrs863224476
gwascentralrs863224476
openSNPrs863224476
23andMers863224476
23andMe allrs863224476
SNP Nexus

SNPshotrs863224476
SNPdbers863224476
MSV3drs863224476
GWAS Ctlgrs863224476
Max Magnitude
ClinVar
Risk rs863224476(;)
Alt rs863224476(;)
Reference rs863224476(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030821delA
CLNSRC
CLNACC RCV000196323.1,