rs796051874

Orientation

plus

Stabilized

plus

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

Make rs796051874(A;A)

Make rs796051874(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

195685

Gene

FAM20C

is a	snp
is	mentioned by
dbSNP	rs796051874
dbSNP (classic)	rs796051874
ClinGen	rs796051874
ebi	rs796051874
HLI	rs796051874
Exac	rs796051874
Gnomad	rs796051874
Varsome	rs796051874
LitVar	rs796051874
Map	rs796051874
PheGenI	rs796051874
Biobank	rs796051874
1000 genomes	rs796051874
hgdp	rs796051874
ensembl	rs796051874
geneview	rs796051874
scholar	rs796051874
google	rs796051874
pharmgkb	rs796051874
gwascentral	rs796051874
openSNP	rs796051874
23andMe	rs796051874
SNPshot	rs796051874
SNPdbe	rs796051874
MSV3d	rs796051874
GWAS Ctlg	rs796051874

Max Magnitude

0

ClinVar
Risk	rs796051874(A;A) rs796051874(C;C)
Alt	rs796051874(A;A) rs796051874(C;C)
Reference	Rs796051874(T;T)
Significance	Pathogenic
Disease	Raine syndrome
Variation	info
Gene	FAM20C
CLNDBN	Raine syndrome
Reversed	0
HGVS	NC_000007.13:g.195685T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023861.3,