rs121909489

Orientation

plus

Stabilized

plus

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

Make rs121909489(C;T)

Make rs121909489(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

126615487

Gene	LMX1B, LOC105376277

is a	snp
is	mentioned by
dbSNP	rs121909489
dbSNP (classic)	rs121909489
ClinGen	rs121909489
ebi	rs121909489
HLI	rs121909489
Exac	rs121909489
Gnomad	rs121909489
Varsome	rs121909489
LitVar	rs121909489
Map	rs121909489
PheGenI	rs121909489
Biobank	rs121909489
1000 genomes	rs121909489
hgdp	rs121909489
ensembl	rs121909489
geneview	rs121909489
scholar	rs121909489
google	rs121909489
pharmgkb	rs121909489
gwascentral	rs121909489
openSNP	rs121909489
23andMe	rs121909489
SNPshot	rs121909489
SNPdbe	rs121909489
MSV3d	rs121909489
GWAS Ctlg	rs121909489

Max Magnitude

0

OMIM	602575
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909489(T;T)
Alt	rs121909489(T;T)
Reference	Rs121909489(C;C)
Significance	Pathogenic
Disease	Nail-patella syndrome
Variation	info
Gene	LMX1B
CLNDBN	Nail-patella syndrome
Reversed	0
HGVS	NC_000009.11:g.129377766C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007420.2,