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rs786204238

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204238(-;-)
Make rs786204238(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89815969
GeneFANCA, SPIRE2
is asnp
is mentioned by
dbSNPrs786204238
ebirs786204238
HLIrs786204238
Exacrs786204238
Varsomers786204238
Maprs786204238
PheGenIrs786204238
hapmaprs786204238
1000 genomesrs786204238
hgdprs786204238
ensemblrs786204238
gopubmedrs786204238
geneviewrs786204238
scholarrs786204238
googlers786204238
pharmgkbrs786204238
gwascentralrs786204238
openSNPrs786204238
23andMers786204238
23andMe allrs786204238
SNP Nexus

SNPshotrs786204238
SNPdbers786204238
MSV3drs786204238
GWAS Ctlgrs786204238
Max Magnitude0
ClinVar
Risk rs786204238(;)
Alt rs786204238(;)
Reference rs786204238(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.89882377delC
CLNSRC
CLNACC RCV000168396.1,