rs121908445

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs121908445(C;C)

Make rs121908445(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

148147542

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs121908445
dbSNP (classic)	rs121908445
ClinGen	rs121908445
ebi	rs121908445
HLI	rs121908445
Exac	rs121908445
Gnomad	rs121908445
Varsome	rs121908445
LitVar	rs121908445
Map	rs121908445
PheGenI	rs121908445
Biobank	rs121908445
1000 genomes	rs121908445
hgdp	rs121908445
ensembl	rs121908445
geneview	rs121908445
scholar	rs121908445
google	rs121908445
pharmgkb	rs121908445
gwascentral	rs121908445
openSNP	rs121908445
23andMe	rs121908445
SNPshot	rs121908445
SNPdbe	rs121908445
MSV3d	rs121908445
GWAS Ctlg	rs121908445

Max Magnitude

0

OMIM	604569
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908445(C;C)
Alt	rs121908445(C;C)
Reference	Rs121908445(T;T)
Significance	Other
Disease	Autism 15 not specified Cortical dysplasia-focal epilepsy syndrome
Variation	info
Gene	CNTNAP2
CLNDBN	Autism 15 not specified Cortical dysplasia-focal epilepsy syndrome
Reversed	0
HGVS	NC_000007.13:g.147844634T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005828.4, RCV000187213.2, RCV000467303.1,