rs766425037

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(I;I)	0	common genotype

Make rs766425037(-;-)

Make rs766425037(-;A)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

38074559

Gene

CYP1B1

is a	snp
is	mentioned by
dbSNP	rs766425037
dbSNP (classic)	rs766425037
ClinGen	rs766425037
ebi	rs766425037
HLI	rs766425037
Exac	rs766425037
Gnomad	rs766425037
Varsome	rs766425037
LitVar	rs766425037
Map	rs766425037
PheGenI	rs766425037
Biobank	rs766425037
1000 genomes	rs766425037
hgdp	rs766425037
ensembl	rs766425037
geneview	rs766425037
scholar	rs766425037
google	rs766425037
pharmgkb	rs766425037
gwascentral	rs766425037
openSNP	rs766425037
23andMe	rs766425037
SNPshot	rs766425037
SNPdbe	rs766425037
MSV3d	rs766425037
GWAS Ctlg	rs766425037

Max Magnitude

0

ClinVar
Risk	rs766425037(-;-)
Alt	rs766425037(-;-)
Reference	Rs766425037(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CYP1B1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.38301702delA
CLNSRC
CLNACC	RCV000255451.1,