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rs1057520605

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520605(G;T)
Make rs1057520605(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47798839
GeneMSH6
is asnp
is mentioned by
dbSNPrs1057520605
dbSNP (old)rs1057520605
ClinGenrs1057520605
ebirs1057520605
HLIrs1057520605
Exacrs1057520605
Gnomadrs1057520605
Varsomers1057520605
Maprs1057520605
PheGenIrs1057520605
Biobankrs1057520605
1000 genomesrs1057520605
hgdprs1057520605
ensemblrs1057520605
gopubmedrs1057520605
geneviewrs1057520605
scholarrs1057520605
googlers1057520605
pharmgkbrs1057520605
gwascentralrs1057520605
openSNPrs1057520605
23andMers1057520605
23andMe allrs1057520605
SNPshotrs1057520605
SNPdbers1057520605
MSV3drs1057520605
GWAS Ctlgrs1057520605
Max Magnitude0
ClinVar
Risk rs1057520605(T;T)
Alt rs1057520605(T;T)
Reference Rs1057520605(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48025978G>T
CLNSRC
CLNACC RCV000441289.1,