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rs1057520600

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520600(C;T)
Make rs1057520600(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position153818111
GeneGATAD2B
is asnp
is mentioned by
dbSNPrs1057520600
dbSNP (old)rs1057520600
ClinGenrs1057520600
ebirs1057520600
HLIrs1057520600
Exacrs1057520600
Gnomadrs1057520600
Varsomers1057520600
Maprs1057520600
PheGenIrs1057520600
Biobankrs1057520600
1000 genomesrs1057520600
hgdprs1057520600
ensemblrs1057520600
gopubmedrs1057520600
geneviewrs1057520600
scholarrs1057520600
googlers1057520600
pharmgkbrs1057520600
gwascentralrs1057520600
openSNPrs1057520600
23andMers1057520600
23andMe allrs1057520600
SNPshotrs1057520600
SNPdbers1057520600
MSV3drs1057520600
GWAS Ctlgrs1057520600
Max Magnitude0
ClinVar
Risk rs1057520600(T;T)
Alt rs1057520600(T;T)
Reference Rs1057520600(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GATAD2B
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.153790587G>A
CLNSRC
CLNACC RCV000419107.1,