rs796051851

Orientation

plus

Stabilized

plus

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

Make rs796051851(C;G)

Make rs796051851(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

248312

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051851
dbSNP (classic)	rs796051851
ClinGen	rs796051851
ebi	rs796051851
HLI	rs796051851
Exac	rs796051851
Gnomad	rs796051851
Varsome	rs796051851
LitVar	rs796051851
Map	rs796051851
PheGenI	rs796051851
Biobank	rs796051851
1000 genomes	rs796051851
hgdp	rs796051851
ensembl	rs796051851
geneview	rs796051851
scholar	rs796051851
google	rs796051851
pharmgkb	rs796051851
gwascentral	rs796051851
openSNP	rs796051851
23andMe	rs796051851
SNPshot	rs796051851
SNPdbe	rs796051851
MSV3d	rs796051851
GWAS Ctlg	rs796051851

Max Magnitude

0

ClinVar
Risk	rs796051851(G;G)
Alt	rs796051851(G;G)
Reference	Rs796051851(C;C)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.288278C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001081.3,