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rs796051997

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051997(A;A)
Make rs796051997(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45508966
GeneMMACHC
is asnp
is mentioned by
dbSNPrs796051997
ebirs796051997
HLIrs796051997
Exacrs796051997
Varsomers796051997
Maprs796051997
PheGenIrs796051997
hapmaprs796051997
1000 genomesrs796051997
hgdprs796051997
ensemblrs796051997
gopubmedrs796051997
geneviewrs796051997
scholarrs796051997
googlers796051997
pharmgkbrs796051997
gwascentralrs796051997
openSNPrs796051997
23andMers796051997
23andMe allrs796051997
SNP Nexus

SNPshotrs796051997
SNPdbers796051997
MSV3drs796051997
GWAS Ctlgrs796051997
Max Magnitude0
ClinVar
Risk rs796051997(A;A)
Alt rs796051997(A;A)
Reference rs796051997(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MMACHC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45974638G>A
CLNSRC
CLNACC RCV000186031.1,