rs267606922

Orientation

minus

Stabilized

minus

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

Make rs267606922(C;G)

Make rs267606922(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

50496039

Gene

NRXN1

is a	snp
is	mentioned by
dbSNP	rs267606922
dbSNP (classic)	rs267606922
ClinGen	rs267606922
ebi	rs267606922
HLI	rs267606922
Exac	rs267606922
Gnomad	rs267606922
Varsome	rs267606922
LitVar	rs267606922
Map	rs267606922
PheGenI	rs267606922
Biobank	rs267606922
1000 genomes	rs267606922
hgdp	rs267606922
ensembl	rs267606922
geneview	rs267606922
scholar	rs267606922
google	rs267606922
pharmgkb	rs267606922
gwascentral	rs267606922
openSNP	rs267606922
23andMe	rs267606922
SNPshot	rs267606922
SNPdbe	rs267606922
MSV3d	rs267606922
GWAS Ctlg	rs267606922

Max Magnitude

0

ClinVar
Risk	rs267606922(G;G)
Alt	rs267606922(G;G)
Reference	Rs267606922(C;C)
Significance	Pathogenic
Disease	Pitt-Hopkins-like syndrome 2
Variation	info
Gene	NRXN1
CLNDBN	Pitt-Hopkins-like syndrome 2
Reversed	1
HGVS	NC_000002.11:g.50723177G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009608.4,