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rs864622257

From SNPedia

Orientationplus
Make rs864622257(-;-)
Make rs864622257(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800119
GeneMSH6
is asnp
is mentioned by
dbSNPrs864622257
ebirs864622257
HLIrs864622257
Exacrs864622257
Varsomers864622257
Maprs864622257
PheGenIrs864622257
hapmaprs864622257
1000 genomesrs864622257
hgdprs864622257
ensemblrs864622257
gopubmedrs864622257
geneviewrs864622257
scholarrs864622257
googlers864622257
pharmgkbrs864622257
gwascentralrs864622257
openSNPrs864622257
23andMers864622257
23andMe allrs864622257
SNP Nexus

SNPshotrs864622257
SNPdbers864622257
MSV3drs864622257
GWAS Ctlgrs864622257
Max Magnitude
ClinVar
Risk rs864622257(;)
Alt rs864622257(;)
Reference rs864622257(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027258delG
CLNSRC
CLNACC RCV000203704.1,