rs1060499782

Orientation

plus

Stabilized

plus

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

Make rs1060499782(-;-)

Make rs1060499782(-;GA)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

232535132

Gene

CHRND

is a	snp
is	mentioned by
dbSNP	rs1060499782
dbSNP (classic)	rs1060499782
ClinGen	rs1060499782
ebi	rs1060499782
HLI	rs1060499782
Exac	rs1060499782
Gnomad	rs1060499782
Varsome	rs1060499782
LitVar	rs1060499782
Map	rs1060499782
PheGenI	rs1060499782
Biobank	rs1060499782
1000 genomes	rs1060499782
hgdp	rs1060499782
ensembl	rs1060499782
geneview	rs1060499782
scholar	rs1060499782
google	rs1060499782
pharmgkb	rs1060499782
gwascentral	rs1060499782
openSNP	rs1060499782
23andMe	rs1060499782
SNPshot	rs1060499782
SNPdbe	rs1060499782
MSV3d	rs1060499782
GWAS Ctlg	rs1060499782

Max Magnitude

0

ClinVar
Risk	rs1060499782(-;-)
Alt	rs1060499782(-;-)
Reference	Rs1060499782(GA;GA)
Significance	Probable-Pathogenic
Disease	Lethal multiple pterygium syndrome
Variation	info
Gene	CHRND
CLNDBN	Lethal multiple pterygium syndrome
Reversed	0
HGVS	NC_000002.11:g.233399842_233399843delGA
CLNSRC
CLNACC	RCV000454340.1,