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rs397516421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516421(A;A)
Make rs397516421(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107701101
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs397516421
ebirs397516421
HLIrs397516421
Exacrs397516421
Varsomers397516421
Maprs397516421
PheGenIrs397516421
hapmaprs397516421
1000 genomesrs397516421
hgdprs397516421
ensemblrs397516421
gopubmedrs397516421
geneviewrs397516421
scholarrs397516421
googlers397516421
pharmgkbrs397516421
gwascentralrs397516421
openSNPrs397516421
23andMers397516421
23andMe allrs397516421
SNP Nexus

SNPshotrs397516421
SNPdbers397516421
MSV3drs397516421
GWAS Ctlgrs397516421
Max Magnitude0
ClinVar
Risk rs397516421(A;A)
Alt rs397516421(A;A)
Reference rs397516421(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SLC26A4
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.107341546G>A
CLNSRC ClinVar
CLNACC RCV000036456.3,