rs387906667

Orientation

plus

Stabilized

plus

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

Make rs387906667(C;C)

Make rs387906667(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

170719822

Gene

PRRX1

is a	snp
is	mentioned by
dbSNP	rs387906667
dbSNP (classic)	rs387906667
ClinGen	rs387906667
ebi	rs387906667
HLI	rs387906667
Exac	rs387906667
Gnomad	rs387906667
Varsome	rs387906667
LitVar	rs387906667
Map	rs387906667
PheGenI	rs387906667
Biobank	rs387906667
1000 genomes	rs387906667
hgdp	rs387906667
ensembl	rs387906667
geneview	rs387906667
scholar	rs387906667
google	rs387906667
pharmgkb	rs387906667
gwascentral	rs387906667
openSNP	rs387906667
23andMe	rs387906667
SNPshot	rs387906667
SNPdbe	rs387906667
MSV3d	rs387906667
GWAS Ctlg	rs387906667

Max Magnitude

0

ClinVar
Risk	rs387906667(C;C)
Alt	rs387906667(C;C)
Reference	Rs387906667(T;T)
Significance	Pathogenic
Disease	Dysgnathia complex
Variation	info
Gene	PRRX1
CLNDBN	Dysgnathia complex
Reversed	0
HGVS	NC_000001.10:g.170688963T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022701.26,