rs796051852

Orientation

plus

Stabilized

plus

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

Make rs796051852(A;A)

Make rs796051852(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

255912

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051852
dbSNP (classic)	rs796051852
ClinGen	rs796051852
ebi	rs796051852
HLI	rs796051852
Exac	rs796051852
Gnomad	rs796051852
Varsome	rs796051852
LitVar	rs796051852
Map	rs796051852
PheGenI	rs796051852
Biobank	rs796051852
1000 genomes	rs796051852
hgdp	rs796051852
ensembl	rs796051852
geneview	rs796051852
scholar	rs796051852
google	rs796051852
pharmgkb	rs796051852
gwascentral	rs796051852
openSNP	rs796051852
23andMe	rs796051852
SNPshot	rs796051852
SNPdbe	rs796051852
MSV3d	rs796051852
GWAS Ctlg	rs796051852

Max Magnitude

0

ClinVar
Risk	rs796051852(A;A)
Alt	rs796051852(A;A)
Reference	Rs796051852(G;G)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.295878G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001082.4,