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rs267606823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606823(C;G)
Make rs267606823(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position75624639
GeneFLVCR2
is asnp
is mentioned by
dbSNPrs267606823
ebirs267606823
HLIrs267606823
Exacrs267606823
Varsomers267606823
Maprs267606823
PheGenIrs267606823
hapmaprs267606823
1000 genomesrs267606823
hgdprs267606823
ensemblrs267606823
gopubmedrs267606823
geneviewrs267606823
scholarrs267606823
googlers267606823
pharmgkbrs267606823
gwascentralrs267606823
openSNPrs267606823
23andMers267606823
23andMe allrs267606823
SNP Nexus

SNPshotrs267606823
SNPdbers267606823
MSV3drs267606823
GWAS Ctlgrs267606823
Max Magnitude0
ClinVar
Risk rs267606823(G;G)
Alt rs267606823(G;G)
Reference rs267606823(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.76090982C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001149.3,