rs387906996

Orientation

minus

Stabilized

minus

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

Make rs387906996(A;A)

Make rs387906996(A;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

125997230

Gene

CDON

is a	snp
is	mentioned by
dbSNP	rs387906996
dbSNP (classic)	rs387906996
ClinGen	rs387906996
ebi	rs387906996
HLI	rs387906996
Exac	rs387906996
Gnomad	rs387906996
Varsome	rs387906996
LitVar	rs387906996
Map	rs387906996
PheGenI	rs387906996
Biobank	rs387906996
1000 genomes	rs387906996
hgdp	rs387906996
ensembl	rs387906996
geneview	rs387906996
scholar	rs387906996
google	rs387906996
pharmgkb	rs387906996
gwascentral	rs387906996
openSNP	rs387906996
23andMe	rs387906996
SNPshot	rs387906996
SNPdbe	rs387906996
MSV3d	rs387906996
GWAS Ctlg	rs387906996

Max Magnitude

0

ClinVar
Risk	rs387906996(A;A)
Alt	rs387906996(A;A)
Reference	Rs387906996(T;T)
Significance	Pathogenic
Disease	Holoprosencephaly 11
Variation	info
Gene	CDON
CLNDBN	Holoprosencephaly 11
Reversed	1
HGVS	NC_000011.9:g.125867125A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023727.4,