rs796051849

Orientation

plus

Stabilized

plus

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

Make rs796051849(G;G)

Make rs796051849(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

255939

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051849
dbSNP (classic)	rs796051849
ClinGen	rs796051849
ebi	rs796051849
HLI	rs796051849
Exac	rs796051849
Gnomad	rs796051849
Varsome	rs796051849
LitVar	rs796051849
Map	rs796051849
PheGenI	rs796051849
Biobank	rs796051849
1000 genomes	rs796051849
hgdp	rs796051849
ensembl	rs796051849
geneview	rs796051849
scholar	rs796051849
google	rs796051849
pharmgkb	rs796051849
gwascentral	rs796051849
openSNP	rs796051849
23andMe	rs796051849
SNPshot	rs796051849
SNPdbe	rs796051849
MSV3d	rs796051849
GWAS Ctlg	rs796051849

Max Magnitude

0

ClinVar
Risk	rs796051849(G;G)
Alt	rs796051849(G;G)
Reference	Rs796051849(T;T)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.295905T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001079.3,