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rs758477536

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs758477536(A;G)
Make rs758477536(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position45500333
GeneCCDC163, MMACHC
is asnp
is mentioned by
dbSNPrs758477536
dbSNP (classic)rs758477536
ClinGenrs758477536
ebirs758477536
HLIrs758477536
Exacrs758477536
Gnomadrs758477536
Varsomers758477536
LitVarrs758477536
Maprs758477536
PheGenIrs758477536
Biobankrs758477536
1000 genomesrs758477536
hgdprs758477536
ensemblrs758477536
geneviewrs758477536
scholarrs758477536
googlers758477536
pharmgkbrs758477536
gwascentralrs758477536
openSNPrs758477536
23andMers758477536
23andMe allrs758477536
SNPshotrs758477536
SNPdbers758477536
MSV3drs758477536
GWAS Ctlgrs758477536
Max Magnitude0
ClinVar
Risk rs758477536(G;G) rs758477536(T;T)
Alt rs758477536(G;G) rs758477536(T;T)
Reference Rs758477536(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MMACHC CCDC163
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45966005A>G
CLNSRC
CLNACC RCV000440436.1,