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rs1057524702

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524702(G;T)
Make rs1057524702(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position155237480
GeneGBA
is asnp
is mentioned by
dbSNPrs1057524702
dbSNP (old)rs1057524702
ClinGenrs1057524702
ebirs1057524702
HLIrs1057524702
Exacrs1057524702
Gnomadrs1057524702
Varsomers1057524702
Maprs1057524702
PheGenIrs1057524702
Biobankrs1057524702
1000 genomesrs1057524702
hgdprs1057524702
ensemblrs1057524702
gopubmedrs1057524702
geneviewrs1057524702
scholarrs1057524702
googlers1057524702
pharmgkbrs1057524702
gwascentralrs1057524702
openSNPrs1057524702
23andMers1057524702
23andMe allrs1057524702
SNPshotrs1057524702
SNPdbers1057524702
MSV3drs1057524702
GWAS Ctlgrs1057524702
Max Magnitude0
ClinVar
Risk rs1057524702(T;T)
Alt rs1057524702(T;T)
Reference Rs1057524702(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GBA
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.155207271C>A
CLNSRC
CLNACC RCV000443344.1,