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rs1057517763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517763(A;A)
Make rs1057517763(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47804920
GeneMSH6
is asnp
is mentioned by
dbSNPrs1057517763
dbSNP (classic)rs1057517763
ClinGenrs1057517763
ebirs1057517763
HLIrs1057517763
Exacrs1057517763
Gnomadrs1057517763
Varsomers1057517763
LitVarrs1057517763
Maprs1057517763
PheGenIrs1057517763
Biobankrs1057517763
1000 genomesrs1057517763
hgdprs1057517763
ensemblrs1057517763
geneviewrs1057517763
scholarrs1057517763
googlers1057517763
pharmgkbrs1057517763
gwascentralrs1057517763
openSNPrs1057517763
23andMers1057517763
23andMe allrs1057517763
SNPshotrs1057517763
SNPdbers1057517763
MSV3drs1057517763
GWAS Ctlgrs1057517763
Max Magnitude0
ClinVar
Risk rs1057517763(A;A)
Alt rs1057517763(A;A)
Reference Rs1057517763(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48032059T>A
CLNSRC
CLNACC RCV000413022.1,