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rs1057521634

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521634(C;C)
Make rs1057521634(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position84017180
GeneSLC38A8
is asnp
is mentioned by
dbSNPrs1057521634
dbSNP (old)rs1057521634
ClinGenrs1057521634
ebirs1057521634
HLIrs1057521634
Exacrs1057521634
Gnomadrs1057521634
Varsomers1057521634
Maprs1057521634
PheGenIrs1057521634
Biobankrs1057521634
1000 genomesrs1057521634
hgdprs1057521634
ensemblrs1057521634
gopubmedrs1057521634
geneviewrs1057521634
scholarrs1057521634
googlers1057521634
pharmgkbrs1057521634
gwascentralrs1057521634
openSNPrs1057521634
23andMers1057521634
23andMe allrs1057521634
SNPshotrs1057521634
SNPdbers1057521634
MSV3drs1057521634
GWAS Ctlgrs1057521634
Max Magnitude0
ClinVar
Risk rs1057521634(C;C)
Alt rs1057521634(C;C)
Reference Rs1057521634(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC38A8
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.84050785A>G
CLNSRC
CLNACC RCV000429596.1,