rs776969714

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs776969714(-;C)

Make rs776969714(C;C)

Reference

GRCh38.p7 38.3/149

Chromosome

4

Position

25145129

Gene

SEPSECS

is a	snp
is	mentioned by
dbSNP	rs776969714
dbSNP (classic)	rs776969714
ClinGen	rs776969714
ebi	rs776969714
HLI	rs776969714
Exac	rs776969714
Gnomad	rs776969714
Varsome	rs776969714
LitVar	rs776969714
Map	rs776969714
PheGenI	rs776969714
Biobank	rs776969714
1000 genomes	rs776969714
hgdp	rs776969714
ensembl	rs776969714
geneview	rs776969714
scholar	rs776969714
google	rs776969714
pharmgkb	rs776969714
gwascentral	rs776969714
openSNP	rs776969714
23andMe	rs776969714
SNPshot	rs776969714
SNPdbe	rs776969714
MSV3d	rs776969714
GWAS Ctlg	rs776969714

Max Magnitude

0

ClinVar
Risk	rs776969714(C;C)
Alt	rs776969714(C;C)
Reference	Rs776969714(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SEPSECS
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.25146752dupC
CLNSRC
CLNACC	RCV000396553.1,