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rs745305932

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745305932(A;G)
Make rs745305932(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position98595424
GeneSLC25A3
is asnp
is mentioned by
dbSNPrs745305932
ebirs745305932
HLIrs745305932
Exacrs745305932
Varsomers745305932
Maprs745305932
PheGenIrs745305932
hapmaprs745305932
1000 genomesrs745305932
hgdprs745305932
ensemblrs745305932
gopubmedrs745305932
geneviewrs745305932
scholarrs745305932
googlers745305932
pharmgkbrs745305932
gwascentralrs745305932
openSNPrs745305932
23andMers745305932
23andMe allrs745305932
SNP Nexus

SNPshotrs745305932
SNPdbers745305932
MSV3drs745305932
GWAS Ctlgrs745305932
Max Magnitude0
ClinVar
Risk rs745305932(G;G)
Alt rs745305932(G;G)
Reference rs745305932(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC25A3
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.98989202A>G
CLNSRC
CLNACC RCV000195488.1,