rs121908423

Orientation

plus

Stabilized

plus

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

Make rs121908423(A;G)

Make rs121908423(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

33017018

Gene

KL

is a	snp
is	mentioned by
dbSNP	rs121908423
dbSNP (classic)	rs121908423
ClinGen	rs121908423
ebi	rs121908423
HLI	rs121908423
Exac	rs121908423
Gnomad	rs121908423
Varsome	rs121908423
LitVar	rs121908423
Map	rs121908423
PheGenI	rs121908423
Biobank	rs121908423
1000 genomes	rs121908423
hgdp	rs121908423
ensembl	rs121908423
geneview	rs121908423
scholar	rs121908423
google	rs121908423
pharmgkb	rs121908423
gwascentral	rs121908423
openSNP	rs121908423
23andMe	rs121908423
SNPshot	rs121908423
SNPdbe	rs121908423
MSV3d	rs121908423
GWAS Ctlg	rs121908423

Max Magnitude

0

OMIM	604824
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908423(G;G)
Alt	rs121908423(G;G)
Reference	Rs121908423(A;A)
Significance	Pathogenic
Disease	Tumoral calcinosis
Variation	info
Gene	LOC101927403 KL
CLNDBN	Tumoral calcinosis, hyperphosphatemic
Reversed	0
HGVS	NC_000013.10:g.33591156A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005675.3,