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rs796051998

From SNPedia

Orientationplus
Geno Mag Summary
(TAC;TAC) 0 common in clinvar
Make rs796051998(-;-)
Make rs796051998(-;TAC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45508323
GeneMMACHC
is asnp
is mentioned by
dbSNPrs796051998
ebirs796051998
HLIrs796051998
Exacrs796051998
Varsomers796051998
Maprs796051998
PheGenIrs796051998
hapmaprs796051998
1000 genomesrs796051998
hgdprs796051998
ensemblrs796051998
gopubmedrs796051998
geneviewrs796051998
scholarrs796051998
googlers796051998
pharmgkbrs796051998
gwascentralrs796051998
openSNPrs796051998
23andMers796051998
23andMe allrs796051998
SNP Nexus

SNPshotrs796051998
SNPdbers796051998
MSV3drs796051998
GWAS Ctlgrs796051998
Max Magnitude0
ClinVar
Risk rs796051998(;)
Alt rs796051998(;)
Reference rs796051998(TAC;TAC)
Significance Pathogenic
Disease not provided
Variation info
Gene MMACHC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45973995_45973997delTAC
CLNSRC
CLNACC RCV000186033.1,