rs397507561

Orientation

minus

Stabilized

minus

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

Make rs397507561(A;G)

Make rs397507561(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35076585

Gene

FANCG

is a	snp
is	mentioned by
dbSNP	rs397507561
dbSNP (classic)	rs397507561
ClinGen	rs397507561
ebi	rs397507561
HLI	rs397507561
Exac	rs397507561
Gnomad	rs397507561
Varsome	rs397507561
LitVar	rs397507561
Map	rs397507561
PheGenI	rs397507561
Biobank	rs397507561
1000 genomes	rs397507561
hgdp	rs397507561
ensembl	rs397507561
geneview	rs397507561
scholar	rs397507561
google	rs397507561
pharmgkb	rs397507561
gwascentral	rs397507561
openSNP	rs397507561
23andMe	rs397507561
SNPshot	rs397507561
SNPdbe	rs397507561
MSV3d	rs397507561
GWAS Ctlg	rs397507561

Max Magnitude

0

ClinVar
Risk	rs397507561(G;G)
Alt	rs397507561(G;G)
Reference	Rs397507561(A;A)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCG
CLNDBN	Fanconi anemia, complementation group G
Reversed	1
HGVS	NC_000009.11:g.35076582T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007108.3,