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rs796051995

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051995(C;T)
Make rs796051995(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45507491
GeneMMACHC
is asnp
is mentioned by
dbSNPrs796051995
ebirs796051995
HLIrs796051995
Exacrs796051995
Varsomers796051995
Maprs796051995
PheGenIrs796051995
hapmaprs796051995
1000 genomesrs796051995
hgdprs796051995
ensemblrs796051995
gopubmedrs796051995
geneviewrs796051995
scholarrs796051995
googlers796051995
pharmgkbrs796051995
gwascentralrs796051995
openSNPrs796051995
23andMers796051995
23andMe allrs796051995
SNP Nexus

SNPshotrs796051995
SNPdbers796051995
MSV3drs796051995
GWAS Ctlgrs796051995
Max Magnitude0
ClinVar
Risk rs796051995(T;T)
Alt rs796051995(T;T)
Reference rs796051995(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MMACHC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45973163C>T
CLNSRC
CLNACC RCV000186024.2,