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rs766567785

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766567785(A;A)
Make rs766567785(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10067267
GeneFANCD2
is asnp
is mentioned by
dbSNPrs766567785
ebirs766567785
HLIrs766567785
Exacrs766567785
Varsomers766567785
Maprs766567785
PheGenIrs766567785
hapmaprs766567785
1000 genomesrs766567785
hgdprs766567785
ensemblrs766567785
gopubmedrs766567785
geneviewrs766567785
scholarrs766567785
googlers766567785
pharmgkbrs766567785
gwascentralrs766567785
openSNPrs766567785
23andMers766567785
23andMe allrs766567785
SNP Nexus

SNPshotrs766567785
SNPdbers766567785
MSV3drs766567785
GWAS Ctlgrs766567785
Max Magnitude0
ClinVar
Risk rs766567785(A;A)
Alt rs766567785(A;A)
Reference rs766567785(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCD2
CLNDBN Fanconi anemia
Reversed 0
HGVS NC_000003.11:g.10108951G>A
CLNSRC
CLNACC RCV000234321.1,