rs121909491

Orientation

plus

Stabilized

plus

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

Make rs121909491(A;A)

Make rs121909491(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

126693250

Gene

LMX1B

is a	snp
is	mentioned by
dbSNP	rs121909491
dbSNP (classic)	rs121909491
ClinGen	rs121909491
ebi	rs121909491
HLI	rs121909491
Exac	rs121909491
Gnomad	rs121909491
Varsome	rs121909491
LitVar	rs121909491
Map	rs121909491
PheGenI	rs121909491
Biobank	rs121909491
1000 genomes	rs121909491
hgdp	rs121909491
ensembl	rs121909491
geneview	rs121909491
scholar	rs121909491
google	rs121909491
pharmgkb	rs121909491
gwascentral	rs121909491
openSNP	rs121909491
23andMe	rs121909491
SNPshot	rs121909491
SNPdbe	rs121909491
MSV3d	rs121909491
GWAS Ctlg	rs121909491

Merged from

Rs28939692

Max Magnitude

0

OMIM	602575
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121909491(A;A)
Alt	rs121909491(A;A)
Reference	Rs121909491(G;G)
Significance	Pathogenic
Disease	Nail-patella syndrome
Variation	info
Gene	LMX1B
CLNDBN	Nail-patella syndrome
Reversed	0
HGVS	NC_000009.11:g.129455529G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007422.2,