rs600753

Orientation

plus

Stabilized

plus

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

Make rs600753(C;C)

Make rs600753(C;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

55466995

Gene	DYX1C1, DYX1C1-CCPG1

is a	snp
is	mentioned by
dbSNP	rs600753
dbSNP (classic)	rs600753
ClinGen	rs600753
ebi	rs600753
HLI	rs600753
Exac	rs600753
Gnomad	rs600753
Varsome	rs600753
LitVar	rs600753
Map	rs600753
PheGenI	rs600753
Biobank	rs600753
1000 genomes	rs600753
hgdp	rs600753
ensembl	rs600753
geneview	rs600753
scholar	rs600753
google	rs600753
pharmgkb	rs600753
gwascentral	rs600753
openSNP	rs600753
23andMe	rs600753
SNPshot	rs600753
SNPdbe	rs600753
MSV3d	rs600753
GWAS Ctlg	rs600753

GMAF

0.4697

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 18288507] Structural genomic variation in ischemic stroke.

[PMID 19240663] Further evidence for DYX1C1 as a susceptibility factor for dyslexia.

ClinVar
Risk	rs600753(C;C)
Alt	rs600753(C;C)
Reference	Rs600753(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	DYX1C1 DYX1C1-CCPG1
CLNDBN	not specified
Reversed	0
HGVS	NC_000015.9:g.55759193T>C
CLNSRC
CLNACC	RCV000242839.1,