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rs267606824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606824(C;T)
Make rs267606824(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position75633653
GeneFLVCR2
is asnp
is mentioned by
dbSNPrs267606824
ebirs267606824
HLIrs267606824
Exacrs267606824
Varsomers267606824
Maprs267606824
PheGenIrs267606824
hapmaprs267606824
1000 genomesrs267606824
hgdprs267606824
ensemblrs267606824
gopubmedrs267606824
geneviewrs267606824
scholarrs267606824
googlers267606824
pharmgkbrs267606824
gwascentralrs267606824
openSNPrs267606824
23andMers267606824
23andMe allrs267606824
SNP Nexus

SNPshotrs267606824
SNPdbers267606824
MSV3drs267606824
GWAS Ctlgrs267606824
Max Magnitude0
ClinVar
Risk rs267606824(T;T)
Alt rs267606824(T;T)
Reference rs267606824(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.76099996C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001150.3,