rs796051875

Orientation

plus

Stabilized

plus

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

Make rs796051875(A;A)

Make rs796051875(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

208909

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051875
dbSNP (classic)	rs796051875
ClinGen	rs796051875
ebi	rs796051875
HLI	rs796051875
Exac	rs796051875
Gnomad	rs796051875
Varsome	rs796051875
LitVar	rs796051875
Map	rs796051875
PheGenI	rs796051875
Biobank	rs796051875
1000 genomes	rs796051875
hgdp	rs796051875
ensembl	rs796051875
geneview	rs796051875
scholar	rs796051875
google	rs796051875
pharmgkb	rs796051875
gwascentral	rs796051875
openSNP	rs796051875
23andMe	rs796051875
SNPshot	rs796051875
SNPdbe	rs796051875
MSV3d	rs796051875
GWAS Ctlg	rs796051875

Max Magnitude

0

ClinVar
Risk	rs796051875(A;A) rs796051875(T;T)
Alt	rs796051875(A;A) rs796051875(T;T)
Reference	Rs796051875(G;G)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.208909G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023862.4,