rs796051855

Orientation

plus

Stabilized

plus

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

Make rs796051855(A;A)

Make rs796051855(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

258645

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051855
dbSNP (classic)	rs796051855
ClinGen	rs796051855
ebi	rs796051855
HLI	rs796051855
Exac	rs796051855
Gnomad	rs796051855
Varsome	rs796051855
LitVar	rs796051855
Map	rs796051855
PheGenI	rs796051855
Biobank	rs796051855
1000 genomes	rs796051855
hgdp	rs796051855
ensembl	rs796051855
geneview	rs796051855
scholar	rs796051855
google	rs796051855
pharmgkb	rs796051855
gwascentral	rs796051855
openSNP	rs796051855
23andMe	rs796051855
SNPshot	rs796051855
SNPdbe	rs796051855
MSV3d	rs796051855
GWAS Ctlg	rs796051855

Max Magnitude

0

ClinVar
Risk	rs796051855(A;A)
Alt	rs796051855(A;A)
Reference	Rs796051855(G;G)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.298611G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001085.4,