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rs772010858

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772010858(-;-)
Make rs772010858(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position183015531
GeneMCCC1
is asnp
is mentioned by
dbSNPrs772010858
ebirs772010858
HLIrs772010858
Exacrs772010858
Varsomers772010858
Maprs772010858
PheGenIrs772010858
hapmaprs772010858
1000 genomesrs772010858
hgdprs772010858
ensemblrs772010858
gopubmedrs772010858
geneviewrs772010858
scholarrs772010858
googlers772010858
pharmgkbrs772010858
gwascentralrs772010858
openSNPrs772010858
23andMers772010858
23andMe allrs772010858
SNP Nexus

SNPshotrs772010858
SNPdbers772010858
MSV3drs772010858
GWAS Ctlgrs772010858
Max Magnitude0
ClinVar
Risk rs772010858(;)
Alt rs772010858(;)
Reference rs772010858(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.182733319delC
CLNSRC
CLNACC RCV000185995.1,