rs794729088

Orientation

plus

Stabilized

plus

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

Make rs794729088(-;-)

Make rs794729088(-;ACAA)

Make rs794729088(ACAA;ACAA)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

77925201

Gene

NEXN

is a	snp
is	mentioned by
dbSNP	rs794729088
dbSNP (classic)	rs794729088
ClinGen	rs794729088
ebi	rs794729088
HLI	rs794729088
Exac	rs794729088
Gnomad	rs794729088
Varsome	rs794729088
LitVar	rs794729088
Map	rs794729088
PheGenI	rs794729088
Biobank	rs794729088
1000 genomes	rs794729088
hgdp	rs794729088
ensembl	rs794729088
geneview	rs794729088
scholar	rs794729088
google	rs794729088
pharmgkb	rs794729088
gwascentral	rs794729088
openSNP	rs794729088
23andMe	rs794729088
SNPshot	rs794729088
SNPdbe	rs794729088
MSV3d	rs794729088
GWAS Ctlg	rs794729088

Max Magnitude

0

ClinVar
Risk	rs794729088(-;-)
Alt	rs794729088(-;-)
Reference	Rs794729088(AAAC;AAAC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NEXN
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.78390886_78390889delACAA
CLNSRC
CLNACC	RCV000183676.2,