rs786204205

Orientation

minus

Stabilized

minus

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

Make rs786204205(G;T)

Make rs786204205(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

35074384

Gene	FANCG, VCP

is a	snp
is	mentioned by
dbSNP	rs786204205
dbSNP (classic)	rs786204205
ClinGen	rs786204205
ebi	rs786204205
HLI	rs786204205
Exac	rs786204205
Gnomad	rs786204205
Varsome	rs786204205
LitVar	rs786204205
Map	rs786204205
PheGenI	rs786204205
Biobank	rs786204205
1000 genomes	rs786204205
hgdp	rs786204205
ensembl	rs786204205
geneview	rs786204205
scholar	rs786204205
google	rs786204205
pharmgkb	rs786204205
gwascentral	rs786204205
openSNP	rs786204205
23andMe	rs786204205
SNPshot	rs786204205
SNPdbe	rs786204205
MSV3d	rs786204205
GWAS Ctlg	rs786204205

Max Magnitude

0

ClinVar
Risk	rs786204205(T;T)
Alt	rs786204205(T;T)
Reference	Rs786204205(G;G)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	VCP FANCG
CLNDBN	Fanconi anemia
Reversed	1
HGVS	NC_000009.11:g.35074381C>A
CLNSRC
CLNACC	RCV000168294.2,