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rs879253970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253970(A;A)
Make rs879253970(A;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position107640956
GenePRPS1
is asnp
is mentioned by
dbSNPrs879253970
dbSNP (classic)rs879253970
ClinGenrs879253970
ebirs879253970
HLIrs879253970
Exacrs879253970
Gnomadrs879253970
Varsomers879253970
LitVarrs879253970
Maprs879253970
PheGenIrs879253970
Biobankrs879253970
1000 genomesrs879253970
hgdprs879253970
ensemblrs879253970
geneviewrs879253970
scholarrs879253970
googlers879253970
pharmgkbrs879253970
gwascentralrs879253970
openSNPrs879253970
23andMers879253970
SNPshotrs879253970
SNPdbers879253970
MSV3drs879253970
GWAS Ctlgrs879253970
Max Magnitude0
ClinVar
Risk rs879253970(A;A)
Alt rs879253970(A;A)
Reference Rs879253970(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRPS1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.106884186G>A
CLNSRC
CLNACC RCV000236738.1,