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rs372968576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372968576(-;-)
Make rs372968576(-;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position56956824
GeneC8B
is asnp
is mentioned by
dbSNPrs372968576
ebirs372968576
HLIrs372968576
Exacrs372968576
Varsomers372968576
Maprs372968576
PheGenIrs372968576
hapmaprs372968576
1000 genomesrs372968576
hgdprs372968576
ensemblrs372968576
gopubmedrs372968576
geneviewrs372968576
scholarrs372968576
googlers372968576
pharmgkbrs372968576
gwascentralrs372968576
openSNPrs372968576
23andMers372968576
23andMe allrs372968576
SNP Nexus

SNPshotrs372968576
SNPdbers372968576
MSV3drs372968576
GWAS Ctlgrs372968576
Max Magnitude0
ClinVar
Risk rs372968576(;)
Alt rs372968576(;)
Reference rs372968576(G;G)
Significance Pathogenic
Disease Complement component 8 deficiency type 2
Variation info
Gene C8B
CLNDBN Complement component 8 deficiency type 2
Reversed 0
HGVS NC_000001.10:g.57422497delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000029240.27,