rs61750414

Orientation

minus

Stabilized

minus

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

Make rs61750414(-;-)

Make rs61750414(-;TC)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

92501914

Gene

PEX1

is a	snp
is	mentioned by
dbSNP	rs61750414
dbSNP (classic)	rs61750414
ClinGen	rs61750414
ebi	rs61750414
HLI	rs61750414
Exac	rs61750414
Gnomad	rs61750414
Varsome	rs61750414
LitVar	rs61750414
Map	rs61750414
PheGenI	rs61750414
Biobank	rs61750414
1000 genomes	rs61750414
hgdp	rs61750414
ensembl	rs61750414
geneview	rs61750414
scholar	rs61750414
google	rs61750414
pharmgkb	rs61750414
gwascentral	rs61750414
openSNP	rs61750414
23andMe	rs61750414
SNPshot	rs61750414
SNPdbe	rs61750414
MSV3d	rs61750414
GWAS Ctlg	rs61750414

Max Magnitude

0

ClinVar
Risk	rs61750414(-;-)
Alt	rs61750414(-;-)
Reference	Rs61750414(TC;TC)
Significance	Probable-Pathogenic
Disease	Zellweger syndrome
Variation	info
Gene	PEX1
CLNDBN	Zellweger syndrome
Reversed	1
HGVS	NC_000007.13:g.92131228_92131229delGA
CLNSRC
CLNACC	RCV000169203.1,