rs267606765

Orientation

plus

Stabilized

plus

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

Make rs267606765(A;A)

Make rs267606765(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

72012084

Gene

DHODH

is a	snp
is	mentioned by
dbSNP	rs267606765
dbSNP (classic)	rs267606765
ClinGen	rs267606765
ebi	rs267606765
HLI	rs267606765
Exac	rs267606765
Gnomad	rs267606765
Varsome	rs267606765
LitVar	rs267606765
Map	rs267606765
PheGenI	rs267606765
Biobank	rs267606765
1000 genomes	rs267606765
hgdp	rs267606765
ensembl	rs267606765
geneview	rs267606765
scholar	rs267606765
google	rs267606765
pharmgkb	rs267606765
gwascentral	rs267606765
openSNP	rs267606765
23andMe	rs267606765
SNPshot	rs267606765
SNPdbe	rs267606765
MSV3d	rs267606765
GWAS Ctlg	rs267606765

Max Magnitude

0

ClinVar
Risk	rs267606765(A;A) rs267606765(C;C)
Alt	rs267606765(A;A) rs267606765(C;C)
Reference	Rs267606765(G;G)
Significance	Pathogenic
Disease	Miller syndrome not specified
Variation	info
Gene	DHODH
CLNDBN	Miller syndrome not specified
Reversed	0
HGVS	NC_000016.9:g.72045983G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018293.27, RCV000386653.1,