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rs267606825

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606825(C;G)
Make rs267606825(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position75641008
GeneFLVCR2
is asnp
is mentioned by
dbSNPrs267606825
ebirs267606825
HLIrs267606825
Exacrs267606825
Varsomers267606825
Maprs267606825
PheGenIrs267606825
hapmaprs267606825
1000 genomesrs267606825
hgdprs267606825
ensemblrs267606825
gopubmedrs267606825
geneviewrs267606825
scholarrs267606825
googlers267606825
pharmgkbrs267606825
gwascentralrs267606825
openSNPrs267606825
23andMers267606825
23andMe allrs267606825
SNP Nexus

SNPshotrs267606825
SNPdbers267606825
MSV3drs267606825
GWAS Ctlgrs267606825
Max Magnitude0
ClinVar
Risk rs267606825(G,T;G,T)
Alt rs267606825(G,T;G,T)
Reference rs267606825(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.76107351C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001145.2,