rs398122375

Orientation

plus

Stabilized

plus

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

Make rs398122375(-;-)

Make rs398122375(-;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

170719753

Gene

PRRX1

is a	snp
is	mentioned by
dbSNP	rs398122375
dbSNP (classic)	rs398122375
ClinGen	rs398122375
ebi	rs398122375
HLI	rs398122375
Exac	rs398122375
Gnomad	rs398122375
Varsome	rs398122375
LitVar	rs398122375
Map	rs398122375
PheGenI	rs398122375
Biobank	rs398122375
1000 genomes	rs398122375
hgdp	rs398122375
ensembl	rs398122375
geneview	rs398122375
scholar	rs398122375
google	rs398122375
pharmgkb	rs398122375
gwascentral	rs398122375
openSNP	rs398122375
23andMe	rs398122375
SNPshot	rs398122375
SNPdbe	rs398122375
MSV3d	rs398122375
GWAS Ctlg	rs398122375

Max Magnitude

0

ClinVar
Risk	rs398122375(-;-)
Alt	rs398122375(-;-)
Reference	Rs398122375(A;A)
Significance	Pathogenic
Disease	Dysgnathia complex
Variation	info
Gene	PRRX1
CLNDBN	Dysgnathia complex
Reversed	0
HGVS	NC_000001.10:g.170688894delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043529.22,