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rs864622556

From SNPedia

Orientationplus
Make rs864622556(-;-)
Make rs864622556(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47410148
GeneMSH2
is asnp
is mentioned by
dbSNPrs864622556
ebirs864622556
HLIrs864622556
Exacrs864622556
Varsomers864622556
Maprs864622556
PheGenIrs864622556
hapmaprs864622556
1000 genomesrs864622556
hgdprs864622556
ensemblrs864622556
gopubmedrs864622556
geneviewrs864622556
scholarrs864622556
googlers864622556
pharmgkbrs864622556
gwascentralrs864622556
openSNPrs864622556
23andMers864622556
23andMe allrs864622556
SNP Nexus

SNPshotrs864622556
SNPdbers864622556
MSV3drs864622556
GWAS Ctlgrs864622556
Max Magnitude
ClinVar
Risk rs864622556(;)
Alt rs864622556(;)
Reference rs864622556(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637287_47637288delAT
CLNSRC
CLNACC RCV000205179.2,