rs398122376

Orientation

plus

Stabilized

plus

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

Make rs398122376(-;AAAA)

Make rs398122376(AAAA;AAAA)

Reference

GRCh38 38.1/141

Chromosome

1

Position

170719753

Gene

PRRX1

is a	snp
is	mentioned by
dbSNP	rs398122376
dbSNP (classic)	rs398122376
ClinGen	rs398122376
ebi	rs398122376
HLI	rs398122376
Exac	rs398122376
Gnomad	rs398122376
Varsome	rs398122376
LitVar	rs398122376
Map	rs398122376
PheGenI	rs398122376
Biobank	rs398122376
1000 genomes	rs398122376
hgdp	rs398122376
ensembl	rs398122376
geneview	rs398122376
scholar	rs398122376
google	rs398122376
pharmgkb	rs398122376
gwascentral	rs398122376
openSNP	rs398122376
23andMe	rs398122376
SNPshot	rs398122376
SNPdbe	rs398122376
MSV3d	rs398122376
GWAS Ctlg	rs398122376

Max Magnitude

0

ClinVar
Risk	rs398122376(AAAA;AAAA)
Alt	rs398122376(AAAA;AAAA)
Reference	Rs398122376(-;-)
Significance	Pathogenic
Disease	Dysgnathia complex
Variation	info
Gene	PRRX1
CLNDBN	Dysgnathia complex
Reversed	0
HGVS	NC_000001.10:g.170688891_170688894dupAAAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043530.28,