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rs1057518410

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518410(C;T)
Make rs1057518410(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position47106062
GeneSETD2
is asnp
is mentioned by
dbSNPrs1057518410
dbSNP (old)rs1057518410
ClinGenrs1057518410
ebirs1057518410
HLIrs1057518410
Exacrs1057518410
Gnomadrs1057518410
Varsomers1057518410
Maprs1057518410
PheGenIrs1057518410
Biobankrs1057518410
1000 genomesrs1057518410
hgdprs1057518410
ensemblrs1057518410
gopubmedrs1057518410
geneviewrs1057518410
scholarrs1057518410
googlers1057518410
pharmgkbrs1057518410
gwascentralrs1057518410
openSNPrs1057518410
23andMers1057518410
23andMe allrs1057518410
SNPshotrs1057518410
SNPdbers1057518410
MSV3drs1057518410
GWAS Ctlgrs1057518410
Max Magnitude0
ClinVar
Risk rs1057518410(T;T)
Alt rs1057518410(T;T)
Reference Rs1057518410(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SETD2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.47147552G>A
CLNSRC
CLNACC RCV000412789.1,