rs61750422

Orientation

minus

Stabilized

minus

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

Make rs61750422(C;T)

Make rs61750422(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

92499808

Gene

PEX1

is a	snp
is	mentioned by
dbSNP	rs61750422
dbSNP (classic)	rs61750422
ClinGen	rs61750422
ebi	rs61750422
HLI	rs61750422
Exac	rs61750422
Gnomad	rs61750422
Varsome	rs61750422
LitVar	rs61750422
Map	rs61750422
PheGenI	rs61750422
Biobank	rs61750422
1000 genomes	rs61750422
hgdp	rs61750422
ensembl	rs61750422
geneview	rs61750422
scholar	rs61750422
google	rs61750422
pharmgkb	rs61750422
gwascentral	rs61750422
openSNP	rs61750422
23andMe	rs61750422
SNPshot	rs61750422
SNPdbe	rs61750422
MSV3d	rs61750422
GWAS Ctlg	rs61750422

Max Magnitude

0

ClinVar
Risk	rs61750422(A;A) rs61750422(G;G) rs61750422(T;T)
Alt	rs61750422(A;A) rs61750422(G;G) rs61750422(T;T)
Reference	Rs61750422(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PEX1
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.92129122G>A
CLNSRC
CLNACC	RCV000254886.1,