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rs398123437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAAGATTGTCGGCAAGTGG;CAAGATTGTCGGCAAGTGG) 0 common in clinvar
Make rs398123437(-;-)
Make rs398123437(-;CAAGATTGTCGGCAAGTGG)
ReferenceGRCh38 38.1/141
Chromosome16
Position88840991
GeneGALNS
is asnp
is mentioned by
dbSNPrs398123437
dbSNP (old)rs398123437
ClinGenrs398123437
ebirs398123437
HLIrs398123437
Exacrs398123437
Gnomadrs398123437
Varsomers398123437
Maprs398123437
PheGenIrs398123437
Biobankrs398123437
1000 genomesrs398123437
hgdprs398123437
ensemblrs398123437
gopubmedrs398123437
geneviewrs398123437
scholarrs398123437
googlers398123437
pharmgkbrs398123437
gwascentralrs398123437
openSNPrs398123437
23andMers398123437
23andMe allrs398123437
SNP Nexus

SNPshotrs398123437
SNPdbers398123437
MSV3drs398123437
GWAS Ctlgrs398123437
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs398123437(CAAGATTGTCGGCAAGTGG;CAAGATTGTCGGCAAGTGG)
Significance Pathogenic
Disease not provided
Variation info
Gene GALNS
CLNDBN not provided
Reversed 1
HGVS NC_000016.10:g.88840991_88841009del19
CLNSRC ClinVar
CLNACC RCV000079035.1,