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rs398123123

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGGGCCAGCCGGCCGCC;GGGGCCAGCCGGCCGCC) 0 common in clinvar
Make rs398123123(-;-)
Make rs398123123(-;GGGGCCAGCCGGCCGCC)
ReferenceGRCh38 38.1/141
Chromosome5
Position78985115
GeneARSB
is asnp
is mentioned by
dbSNPrs398123123
ebirs398123123
HLIrs398123123
Exacrs398123123
Varsomers398123123
Maprs398123123
PheGenIrs398123123
hapmaprs398123123
1000 genomesrs398123123
hgdprs398123123
ensemblrs398123123
gopubmedrs398123123
geneviewrs398123123
scholarrs398123123
googlers398123123
pharmgkbrs398123123
gwascentralrs398123123
openSNPrs398123123
23andMers398123123
23andMe allrs398123123
SNP Nexus

SNPshotrs398123123
SNPdbers398123123
MSV3drs398123123
GWAS Ctlgrs398123123
Max Magnitude0
ClinVar
Risk rs398123123(;)
Alt rs398123123(;)
Reference rs398123123(GGGGCCAGCCGGCCGCC;GGGGCCAGCCGGCCGCC)
Significance Pathogenic
Disease not provided
Variation info
Gene ARSB
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.78280938_78280954del17
CLNSRC ClinVar
CLNACC RCV000078000.4,