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rs587776640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGCGGTA;GGCGGTA) 0 common in clinvar
Make rs587776640(-;-)
Make rs587776640(-;GGCGGTA)
ReferenceGRCh38 38.1/142
Chromosome9
Position35077267
GeneFANCG
is asnp
is mentioned by
dbSNPrs587776640
ebirs587776640
HLIrs587776640
Exacrs587776640
Varsomers587776640
Maprs587776640
PheGenIrs587776640
hapmaprs587776640
1000 genomesrs587776640
hgdprs587776640
ensemblrs587776640
gopubmedrs587776640
geneviewrs587776640
scholarrs587776640
googlers587776640
pharmgkbrs587776640
gwascentralrs587776640
openSNPrs587776640
23andMers587776640
23andMe allrs587776640
SNP Nexus

SNPshotrs587776640
SNPdbers587776640
MSV3drs587776640
GWAS Ctlgrs587776640
Max Magnitude0
ClinVar
Risk rs587776640(;)
Alt rs587776640(;)
Reference rs587776640(GGCGGTA;GGCGGTA)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCG
CLNDBN Fanconi anemia, complementation group G
Reversed 0
HGVS NC_000009.11:g.35077264_35077270delGGCGGTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007111.2,