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rs886039425

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039425(C;T)
Make rs886039425(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position149576443
GeneMMADHC
is asnp
is mentioned by
dbSNPrs886039425
dbSNP (classic)rs886039425
ClinGenrs886039425
ebirs886039425
HLIrs886039425
Exacrs886039425
Gnomadrs886039425
Varsomers886039425
LitVarrs886039425
Maprs886039425
PheGenIrs886039425
Biobankrs886039425
1000 genomesrs886039425
hgdprs886039425
ensemblrs886039425
geneviewrs886039425
scholarrs886039425
googlers886039425
pharmgkbrs886039425
gwascentralrs886039425
openSNPrs886039425
23andMers886039425
23andMe allrs886039425
SNPshotrs886039425
SNPdbers886039425
MSV3drs886039425
GWAS Ctlgrs886039425
Max Magnitude0
ClinVar
Risk rs886039425(T;T)
Alt rs886039425(T;T)
Reference Rs886039425(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MMADHC
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.150432957G>A
CLNSRC
CLNACC RCV000255676.1,