rs121909490

Orientation

plus

Stabilized

plus

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

Make rs121909490(C;T)

Make rs121909490(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

126693273

Gene

LMX1B

is a	snp
is	mentioned by
dbSNP	rs121909490
dbSNP (classic)	rs121909490
ClinGen	rs121909490
ebi	rs121909490
HLI	rs121909490
Exac	rs121909490
Gnomad	rs121909490
Varsome	rs121909490
LitVar	rs121909490
Map	rs121909490
PheGenI	rs121909490
Biobank	rs121909490
1000 genomes	rs121909490
hgdp	rs121909490
ensembl	rs121909490
geneview	rs121909490
scholar	rs121909490
google	rs121909490
pharmgkb	rs121909490
gwascentral	rs121909490
openSNP	rs121909490
23andMe	rs121909490
SNPshot	rs121909490
SNPdbe	rs121909490
MSV3d	rs121909490
GWAS Ctlg	rs121909490

Max Magnitude

0

OMIM	602575
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909490(T;T)
Alt	rs121909490(T;T)
Reference	Rs121909490(C;C)
Significance	Pathogenic
Disease	Nail-patella syndrome not provided
Variation	info
Gene	LMX1B
CLNDBN	Nail-patella syndrome not provided
Reversed	0
HGVS	NC_000009.11:g.129455552C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007421.2, RCV000414681.1,