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rs796052000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCAA;CCAA) 0 common in clinvar
Make rs796052000(-;-)
Make rs796052000(-;AACC)
Make rs796052000(AACC;AACC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45508263
GeneMMACHC
is asnp
is mentioned by
dbSNPrs796052000
ClinGenrs796052000
ebirs796052000
HLIrs796052000
Exacrs796052000
Varsomers796052000
Maprs796052000
PheGenIrs796052000
hapmaprs796052000
1000 genomesrs796052000
hgdprs796052000
ensemblrs796052000
gopubmedrs796052000
geneviewrs796052000
scholarrs796052000
googlers796052000
pharmgkbrs796052000
gwascentralrs796052000
openSNPrs796052000
23andMers796052000
23andMe allrs796052000
SNP Nexus

SNPshotrs796052000
SNPdbers796052000
MSV3drs796052000
GWAS Ctlgrs796052000
Max Magnitude0
ClinVar
Risk rs796052000(-;-) Rs796052000(CCAA;CCAA)
Alt rs796052000(-;-) Rs796052000(CCAA;CCAA)
Reference rs796052000(AACC;AACC)
Significance Pathogenic
Disease not provided
Variation info
Gene MMACHC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45973935_45973938delAACC
CLNSRC
CLNACC RCV000186035.1,