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rs786203570

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203570(A;A)
Make rs786203570(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31327751
GeneNF1
is asnp
is mentioned by
dbSNPrs786203570
ebirs786203570
HLIrs786203570
Exacrs786203570
Varsomers786203570
Maprs786203570
PheGenIrs786203570
hapmaprs786203570
1000 genomesrs786203570
hgdprs786203570
ensemblrs786203570
gopubmedrs786203570
geneviewrs786203570
scholarrs786203570
googlers786203570
pharmgkbrs786203570
gwascentralrs786203570
openSNPrs786203570
23andMers786203570
23andMe allrs786203570
SNP Nexus

SNPshotrs786203570
SNPdbers786203570
MSV3drs786203570
GWAS Ctlgrs786203570
Max Magnitude0
ClinVar
Risk rs786203570(A,T;A,T)
Alt rs786203570(A,T;A,T)
Reference rs786203570(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Neurofibromatosis
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29654769C>A; NC_000017.10:g.29654769C>T
CLNSRC
CLNACC RCV000166948.1, RCV000206167.2,