rs121909492

Orientation

plus

Stabilized

plus

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

Make rs121909492(C;T)

Make rs121909492(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

126693527

Gene

LMX1B

is a	snp
is	mentioned by
dbSNP	rs121909492
dbSNP (classic)	rs121909492
ClinGen	rs121909492
ebi	rs121909492
HLI	rs121909492
Exac	rs121909492
Gnomad	rs121909492
Varsome	rs121909492
LitVar	rs121909492
Map	rs121909492
PheGenI	rs121909492
Biobank	rs121909492
1000 genomes	rs121909492
hgdp	rs121909492
ensembl	rs121909492
geneview	rs121909492
scholar	rs121909492
google	rs121909492
pharmgkb	rs121909492
gwascentral	rs121909492
openSNP	rs121909492
23andMe	rs121909492
SNPshot	rs121909492
SNPdbe	rs121909492
MSV3d	rs121909492
GWAS Ctlg	rs121909492

Max Magnitude

0

OMIM	602575
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121909492(T;T)
Alt	rs121909492(T;T)
Reference	Rs121909492(C;C)
Significance	Pathogenic
Disease	Nail-patella syndrome
Variation	info
Gene	LMX1B
CLNDBN	Nail-patella syndrome
Reversed	0
HGVS	NC_000009.11:g.129455806C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007425.2,