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rs267606822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606822(C;G)
Make rs267606822(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position75639419
GeneFLVCR2
is asnp
is mentioned by
dbSNPrs267606822
ebirs267606822
HLIrs267606822
Exacrs267606822
Varsomers267606822
Maprs267606822
PheGenIrs267606822
hapmaprs267606822
1000 genomesrs267606822
hgdprs267606822
ensemblrs267606822
gopubmedrs267606822
geneviewrs267606822
scholarrs267606822
googlers267606822
pharmgkbrs267606822
gwascentralrs267606822
openSNPrs267606822
23andMers267606822
23andMe allrs267606822
SNP Nexus

SNPshotrs267606822
SNPdbers267606822
MSV3drs267606822
GWAS Ctlgrs267606822
Max Magnitude0
ClinVar
Risk rs267606822(G;G)
Alt rs267606822(G;G)
Reference rs267606822(C;C)
Significance Pathogenic
Disease Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
Variation info
Gene FLVCR2
CLNDBN Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
Reversed 0
HGVS NC_000014.8:g.76105762C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001147.3,