rs149616199

Orientation

plus

Stabilized

plus

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

Make rs149616199(C;G)

Make rs149616199(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35075278

Gene

FANCG

is a	snp
is	mentioned by
dbSNP	rs149616199
dbSNP (classic)	rs149616199
ClinGen	rs149616199
ebi	rs149616199
HLI	rs149616199
Exac	rs149616199
Gnomad	rs149616199
Varsome	rs149616199
LitVar	rs149616199
Map	rs149616199
PheGenI	rs149616199
Biobank	rs149616199
1000 genomes	rs149616199
hgdp	rs149616199
ensembl	rs149616199
geneview	rs149616199
scholar	rs149616199
google	rs149616199
pharmgkb	rs149616199
gwascentral	rs149616199
openSNP	rs149616199
23andMe	rs149616199
SNPshot	rs149616199
SNPdbe	rs149616199
MSV3d	rs149616199
GWAS Ctlg	rs149616199

Max Magnitude

0

ClinVar
Risk	rs149616199(G;G)
Alt	rs149616199(G;G)
Reference	Rs149616199(C;C)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCG
CLNDBN	Fanconi anemia, complementation group G
Reversed	0
HGVS	NC_000009.11:g.35075275C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007109.3,