rs104894222

Orientation

minus

Stabilized

minus

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

Make rs104894222(C;G)

Make rs104894222(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

22625484

Gene	FANCF, GAS2

is a	snp
is	mentioned by
dbSNP	rs104894222
dbSNP (classic)	rs104894222
ClinGen	rs104894222
ebi	rs104894222
HLI	rs104894222
Exac	rs104894222
Gnomad	rs104894222
Varsome	rs104894222
LitVar	rs104894222
Map	rs104894222
PheGenI	rs104894222
Biobank	rs104894222
1000 genomes	rs104894222
hgdp	rs104894222
ensembl	rs104894222
geneview	rs104894222
scholar	rs104894222
google	rs104894222
pharmgkb	rs104894222
gwascentral	rs104894222
openSNP	rs104894222
23andMe	rs104894222
SNPshot	rs104894222
SNPdbe	rs104894222
MSV3d	rs104894222
GWAS Ctlg	rs104894222

Max Magnitude

0

OMIM	603467
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894222(G;G)
Alt	rs104894222(G;G)
Reference	Rs104894222(C;C)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCF
CLNDBN	Fanconi anemia, complementation group F
Reversed	1
HGVS	NC_000011.9:g.22647030G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006716.2,