rs121909761

Orientation

plus

Stabilized

plus

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

Make rs121909761(A;A)

Make rs121909761(A;C)

Reference

GRCh38 38.1/141

Chromosome

5

Position

90705508

Gene

ADGRV1

is a	snp
is	mentioned by
dbSNP	rs121909761
dbSNP (classic)	rs121909761
ClinGen	rs121909761
ebi	rs121909761
HLI	rs121909761
Exac	rs121909761
Gnomad	rs121909761
Varsome	rs121909761
LitVar	rs121909761
Map	rs121909761
PheGenI	rs121909761
Biobank	rs121909761
1000 genomes	rs121909761
hgdp	rs121909761
ensembl	rs121909761
geneview	rs121909761
scholar	rs121909761
google	rs121909761
pharmgkb	rs121909761
gwascentral	rs121909761
openSNP	rs121909761
23andMe	rs121909761
SNPshot	rs121909761
SNPdbe	rs121909761
MSV3d	rs121909761
GWAS Ctlg	rs121909761

Max Magnitude

0

OMIM	602851
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909761(A;A)
Alt	rs121909761(A;A)
Reference	Rs121909761(C;C)
Significance	Pathogenic
Disease	Febrile seizures
Variation	info
Gene	ADGRV1 GPR98
CLNDBN	Febrile seizures, familial, 4
Reversed	0
HGVS	NC_000005.9:g.90001325C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007199.4,