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rs863224207

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224207(A;A)
Make rs863224207(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position185145023
GeneSLC25A4
is asnp
is mentioned by
dbSNPrs863224207
ebirs863224207
HLIrs863224207
Exacrs863224207
Varsomers863224207
Maprs863224207
PheGenIrs863224207
hapmaprs863224207
1000 genomesrs863224207
hgdprs863224207
ensemblrs863224207
gopubmedrs863224207
geneviewrs863224207
scholarrs863224207
googlers863224207
pharmgkbrs863224207
gwascentralrs863224207
openSNPrs863224207
23andMers863224207
23andMe allrs863224207
SNP Nexus

SNPshotrs863224207
SNPdbers863224207
MSV3drs863224207
GWAS Ctlgrs863224207
Max Magnitude0
ClinVar
Risk rs863224207(A;A)
Alt rs863224207(A;A)
Reference rs863224207(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SLC25A4
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.186066177G>A
CLNSRC
CLNACC RCV000196570.2,