rs587777303

Orientation

plus

Stabilized

minus

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

Make rs587777303(C;C)

Make rs587777303(C;T)

Reference

GRCh38 38.1/142

Chromosome

6

Position

166165800

Gene

T

is a	snp
is	mentioned by
dbSNP	rs587777303
dbSNP (classic)	rs587777303
ClinGen	rs587777303
ebi	rs587777303
HLI	rs587777303
Exac	rs587777303
Gnomad	rs587777303
Varsome	rs587777303
LitVar	rs587777303
Map	rs587777303
PheGenI	rs587777303
Biobank	rs587777303
1000 genomes	rs587777303
hgdp	rs587777303
ensembl	rs587777303
geneview	rs587777303
scholar	rs587777303
google	rs587777303
pharmgkb	rs587777303
gwascentral	rs587777303
openSNP	rs587777303
23andMe	rs587777303
SNPshot	rs587777303
SNPdbe	rs587777303
MSV3d	rs587777303
GWAS Ctlg	rs587777303

Max Magnitude

0

ClinVar
Risk	rs587777303(C;C) Rs587777303(T;T)
Alt	rs587777303(C;C) Rs587777303(T;T)
Reference	Rs587777303(A;A)
Significance	Pathogenic
Disease	Sacral agenesis with vertebral anomalies
Variation	info
Gene	T
CLNDBN	Sacral agenesis with vertebral anomalies
Reversed	1
HGVS	NC_000006.11:g.166579288T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000114433.3,