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rs140522266

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140522266(C;C)
Make rs140522266(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45508806
GeneMMACHC
is asnp
is mentioned by
dbSNPrs140522266
ebirs140522266
HLIrs140522266
Exacrs140522266
Varsomers140522266
Maprs140522266
PheGenIrs140522266
hapmaprs140522266
1000 genomesrs140522266
hgdprs140522266
ensemblrs140522266
gopubmedrs140522266
geneviewrs140522266
scholarrs140522266
googlers140522266
pharmgkbrs140522266
gwascentralrs140522266
openSNPrs140522266
23andMers140522266
23andMe allrs140522266
SNP Nexus

SNPshotrs140522266
SNPdbers140522266
MSV3drs140522266
GWAS Ctlgrs140522266
Max Magnitude0
ClinVar
Risk rs140522266(A,C;A,C)
Alt rs140522266(A,C;A,C)
Reference rs140522266(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MMACHC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45974478G>A; NC_000001.10:g.45974478G>C
CLNSRC
CLNACC RCV000186029.1, RCV000186028.2,