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rs886037851

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886037851(A;A)
Make rs886037851(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position171813452
GeneSLC25A12
is asnp
is mentioned by
dbSNPrs886037851
dbSNP (classic)rs886037851
ClinGenrs886037851
ebirs886037851
HLIrs886037851
Exacrs886037851
Gnomadrs886037851
Varsomers886037851
LitVarrs886037851
Maprs886037851
PheGenIrs886037851
Biobankrs886037851
1000 genomesrs886037851
hgdprs886037851
ensemblrs886037851
geneviewrs886037851
scholarrs886037851
googlers886037851
pharmgkbrs886037851
gwascentralrs886037851
openSNPrs886037851
23andMers886037851
23andMe allrs886037851
SNPshotrs886037851
SNPdbers886037851
MSV3drs886037851
GWAS Ctlgrs886037851
Max Magnitude0
ClinVar
Risk rs886037851(A;A)
Alt rs886037851(A;A)
Reference Rs886037851(G;G)
Significance Pathogenic
Disease Hypomyelination
Variation info
Gene SLC25A12
CLNDBN Hypomyelination, global cerebral
Reversed 1
HGVS NC_000002.11:g.172669962C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239515.1,