rs104893988

Orientation

plus

Stabilized

plus

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

Make rs104893988(A;A)

Make rs104893988(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

45512277

Gene

RUNX2

is a	snp
is	mentioned by
dbSNP	rs104893988
dbSNP (classic)	rs104893988
ClinGen	rs104893988
ebi	rs104893988
HLI	rs104893988
Exac	rs104893988
Gnomad	rs104893988
Varsome	rs104893988
LitVar	rs104893988
Map	rs104893988
PheGenI	rs104893988
Biobank	rs104893988
1000 genomes	rs104893988
hgdp	rs104893988
ensembl	rs104893988
geneview	rs104893988
scholar	rs104893988
google	rs104893988
pharmgkb	rs104893988
gwascentral	rs104893988
openSNP	rs104893988
23andMe	rs104893988
SNPshot	rs104893988
SNPdbe	rs104893988
MSV3d	rs104893988
GWAS Ctlg	rs104893988

Max Magnitude

0

OMIM	600211
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104893988(A;A)
Alt	rs104893988(A;A)
Reference	Rs104893988(G;G)
Significance	Pathogenic
Disease	Cleidocranial dysostosis
Variation	info
Gene	RUNX2
CLNDBN	Cleidocranial dysostosis
Reversed	0
HGVS	NC_000006.11:g.45480014G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009879.4,