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rs1057522013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057522013(C;G)
Make rs1057522013(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position46196771
GenePOMGNT1, TSPAN1
is asnp
is mentioned by
dbSNPrs1057522013
dbSNP (classic)rs1057522013
ClinGenrs1057522013
ebirs1057522013
HLIrs1057522013
Exacrs1057522013
Gnomadrs1057522013
Varsomers1057522013
LitVarrs1057522013
Maprs1057522013
PheGenIrs1057522013
Biobankrs1057522013
1000 genomesrs1057522013
hgdprs1057522013
ensemblrs1057522013
geneviewrs1057522013
scholarrs1057522013
googlers1057522013
pharmgkbrs1057522013
gwascentralrs1057522013
openSNPrs1057522013
23andMers1057522013
23andMe allrs1057522013
SNPshotrs1057522013
SNPdbers1057522013
MSV3drs1057522013
GWAS Ctlgrs1057522013
Max Magnitude0
ClinVar
Risk rs1057522013(G;G)
Alt rs1057522013(G;G)
Reference Rs1057522013(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POMGNT1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.46662443G>C
CLNSRC
CLNACC RCV000428665.1,