rs121434426

Orientation

minus

Stabilized

minus

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

Make rs121434426(C;T)

Make rs121434426(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35076442

Gene

FANCG

is a	snp
is	mentioned by
dbSNP	rs121434426
dbSNP (classic)	rs121434426
ClinGen	rs121434426
ebi	rs121434426
HLI	rs121434426
Exac	rs121434426
Gnomad	rs121434426
Varsome	rs121434426
LitVar	rs121434426
Map	rs121434426
PheGenI	rs121434426
Biobank	rs121434426
1000 genomes	rs121434426
hgdp	rs121434426
ensembl	rs121434426
geneview	rs121434426
scholar	rs121434426
google	rs121434426
pharmgkb	rs121434426
gwascentral	rs121434426
openSNP	rs121434426
23andMe	rs121434426
SNPshot	rs121434426
SNPdbe	rs121434426
MSV3d	rs121434426
GWAS Ctlg	rs121434426

Max Magnitude

0

OMIM	602956
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121434426(T;T)
Alt	rs121434426(T;T)
Reference	Rs121434426(C;C)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCG
CLNDBN	Fanconi anemia, complementation group G
Reversed	1
HGVS	NC_000009.11:g.35076439G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007107.2,