rs796051853

Orientation

plus

Stabilized

plus

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

Make rs796051853(A;G)

Make rs796051853(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

257003

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051853
dbSNP (classic)	rs796051853
ClinGen	rs796051853
ebi	rs796051853
HLI	rs796051853
Exac	rs796051853
Gnomad	rs796051853
Varsome	rs796051853
LitVar	rs796051853
Map	rs796051853
PheGenI	rs796051853
Biobank	rs796051853
1000 genomes	rs796051853
hgdp	rs796051853
ensembl	rs796051853
geneview	rs796051853
scholar	rs796051853
google	rs796051853
pharmgkb	rs796051853
gwascentral	rs796051853
openSNP	rs796051853
23andMe	rs796051853
SNPshot	rs796051853
SNPdbe	rs796051853
MSV3d	rs796051853
GWAS Ctlg	rs796051853

Max Magnitude

0

ClinVar
Risk	rs796051853(G;G)
Alt	rs796051853(G;G)
Reference	Rs796051853(A;A)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.296969A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001083.4,