Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204211

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204211(A;A)
Make rs786204211(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31232879
GeneNF1
is asnp
is mentioned by
dbSNPrs786204211
ebirs786204211
HLIrs786204211
Exacrs786204211
Varsomers786204211
Maprs786204211
PheGenIrs786204211
hapmaprs786204211
1000 genomesrs786204211
hgdprs786204211
ensemblrs786204211
gopubmedrs786204211
geneviewrs786204211
scholarrs786204211
googlers786204211
pharmgkbrs786204211
gwascentralrs786204211
openSNPrs786204211
23andMers786204211
23andMe allrs786204211
SNP Nexus

SNPshotrs786204211
SNPdbers786204211
MSV3drs786204211
GWAS Ctlgrs786204211
Max Magnitude0
ClinVar
Risk rs786204211(A;A)
Alt rs786204211(A;A)
Reference rs786204211(T;T)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29559897T>A
CLNSRC
CLNACC RCV000168309.2,