rs113994158

Orientation

plus

Stabilized

plus

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

Make rs113994158(-;ACCG)

Make rs113994158(ACCG;ACCG)

Reference

GRCh38 38.1/141

Chromosome

15

Position

89776860

Gene

MESP2

is a	snp
is	mentioned by
dbSNP	rs113994158
dbSNP (classic)	rs113994158
ClinGen	rs113994158
ebi	rs113994158
HLI	rs113994158
Exac	rs113994158
Gnomad	rs113994158
Varsome	rs113994158
LitVar	rs113994158
Map	rs113994158
PheGenI	rs113994158
Biobank	rs113994158
1000 genomes	rs113994158
hgdp	rs113994158
ensembl	rs113994158
geneview	rs113994158
scholar	rs113994158
google	rs113994158
pharmgkb	rs113994158
gwascentral	rs113994158
openSNP	rs113994158
23andMe	rs113994158
SNPshot	rs113994158
SNPdbe	rs113994158
MSV3d	rs113994158
GWAS Ctlg	rs113994158

Max Magnitude

0

OMIM	605195
Desc
Variant	0001
Related	also

ClinVar
Risk	rs113994158(CCGA;CCGA)
Alt	rs113994158(CCGA;CCGA)
Reference	Rs113994158(-;-)
Significance	Pathogenic
Disease	Spondylocostal dysostosis 2
Variation	info
Gene	MESP2
CLNDBN	Spondylocostal dysostosis 2
Reversed	0
HGVS	NC_000015.9:g.90320088_90320091dupACCG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005492.5,