rs267606823

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs267606823(C;G)

Make rs267606823(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

75624639

Gene

FLVCR2

is a	snp
is	mentioned by
dbSNP	rs267606823
dbSNP (classic)	rs267606823
ClinGen	rs267606823
ebi	rs267606823
HLI	rs267606823
Exac	rs267606823
Gnomad	rs267606823
Varsome	rs267606823
LitVar	rs267606823
Map	rs267606823
PheGenI	rs267606823
Biobank	rs267606823
1000 genomes	rs267606823
hgdp	rs267606823
ensembl	rs267606823
geneview	rs267606823
scholar	rs267606823
google	rs267606823
pharmgkb	rs267606823
gwascentral	rs267606823
openSNP	rs267606823
23andMe	rs267606823
SNPshot	rs267606823
SNPdbe	rs267606823
MSV3d	rs267606823
GWAS Ctlg	rs267606823

Max Magnitude

0

ClinVar
Risk	rs267606823(G;G)
Alt	rs267606823(G;G)
Reference	Rs267606823(C;C)
Significance	Other
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 UniProtKB (protein)
CLNACC	RCV000001149.4,