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rs1057518327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518327(-;-)
Make rs1057518327(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position149981424
GeneSLC26A2
is asnp
is mentioned by
dbSNPrs1057518327
dbSNP (classic)rs1057518327
ClinGenrs1057518327
ebirs1057518327
HLIrs1057518327
Exacrs1057518327
Gnomadrs1057518327
Varsomers1057518327
LitVarrs1057518327
Maprs1057518327
PheGenIrs1057518327
Biobankrs1057518327
1000 genomesrs1057518327
hgdprs1057518327
ensemblrs1057518327
geneviewrs1057518327
scholarrs1057518327
googlers1057518327
pharmgkbrs1057518327
gwascentralrs1057518327
openSNPrs1057518327
23andMers1057518327
23andMe allrs1057518327
SNPshotrs1057518327
SNPdbers1057518327
MSV3drs1057518327
GWAS Ctlgrs1057518327
Max Magnitude0
ClinVar
Risk rs1057518327(-;-)
Alt rs1057518327(-;-)
Reference Rs1057518327(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC26A2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.149360987delG
CLNSRC
CLNACC RCV000413986.1,