Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517764

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517764(-;T)
Make rs1057517764(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47805634
GeneMSH6
is asnp
is mentioned by
dbSNPrs1057517764
dbSNP (old)rs1057517764
ClinGenrs1057517764
ebirs1057517764
HLIrs1057517764
Exacrs1057517764
Gnomadrs1057517764
Varsomers1057517764
Maprs1057517764
PheGenIrs1057517764
Biobankrs1057517764
1000 genomesrs1057517764
hgdprs1057517764
ensemblrs1057517764
gopubmedrs1057517764
geneviewrs1057517764
scholarrs1057517764
googlers1057517764
pharmgkbrs1057517764
gwascentralrs1057517764
openSNPrs1057517764
23andMers1057517764
23andMe allrs1057517764
SNPshotrs1057517764
SNPdbers1057517764
MSV3drs1057517764
GWAS Ctlgrs1057517764
Max Magnitude0
ClinVar
Risk rs1057517764(T;T)
Alt rs1057517764(T;T)
Reference Rs1057517764(-;-)
Significance Pathogenic
Disease not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48032773dupT
CLNSRC
CLNACC RCV000413655.1, RCV000460316.1, RCV000490868.1,