Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518194

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TCC;TCC) 0 common in clinvar
Make rs1057518194(-;-)
Make rs1057518194(-;TCC)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position48905270
GeneSLC35A2
is asnp
is mentioned by
dbSNPrs1057518194
dbSNP (old)rs1057518194
ClinGenrs1057518194
ebirs1057518194
HLIrs1057518194
Exacrs1057518194
Gnomadrs1057518194
Varsomers1057518194
Maprs1057518194
PheGenIrs1057518194
Biobankrs1057518194
1000 genomesrs1057518194
hgdprs1057518194
ensemblrs1057518194
gopubmedrs1057518194
geneviewrs1057518194
scholarrs1057518194
googlers1057518194
pharmgkbrs1057518194
gwascentralrs1057518194
openSNPrs1057518194
23andMers1057518194
23andMe allrs1057518194
SNPshotrs1057518194
SNPdbers1057518194
MSV3drs1057518194
GWAS Ctlgrs1057518194
Max Magnitude0
ClinVar
Risk rs1057518194(-;-)
Alt rs1057518194(-;-)
Reference Rs1057518194(TCC;TCC)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC35A2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.48762547_48762549delGGA
CLNSRC
CLNACC RCV000414069.1,