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rs1057524912

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057524912(-;T)
Make rs1057524912(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47791068
GeneMSH6
is asnp
is mentioned by
dbSNPrs1057524912
dbSNP (old)rs1057524912
ClinGenrs1057524912
ebirs1057524912
HLIrs1057524912
Exacrs1057524912
Gnomadrs1057524912
Varsomers1057524912
Maprs1057524912
PheGenIrs1057524912
Biobankrs1057524912
1000 genomesrs1057524912
hgdprs1057524912
ensemblrs1057524912
gopubmedrs1057524912
geneviewrs1057524912
scholarrs1057524912
googlers1057524912
pharmgkbrs1057524912
gwascentralrs1057524912
openSNPrs1057524912
23andMers1057524912
23andMe allrs1057524912
SNPshotrs1057524912
SNPdbers1057524912
MSV3drs1057524912
GWAS Ctlgrs1057524912
Max Magnitude0
ClinVar
Risk rs1057524912(T;T)
Alt rs1057524912(T;T)
Reference Rs1057524912(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48018207dupT
CLNSRC
CLNACC RCV000445393.1,