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

rs768638173

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768638173(C;T)
Make rs768638173(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31226474
GeneNF1
is asnp
is mentioned by
dbSNPrs768638173
ebirs768638173
HLIrs768638173
Exacrs768638173
Varsomers768638173
Maprs768638173
PheGenIrs768638173
hapmaprs768638173
1000 genomesrs768638173
hgdprs768638173
ensemblrs768638173
gopubmedrs768638173
geneviewrs768638173
scholarrs768638173
googlers768638173
pharmgkbrs768638173
gwascentralrs768638173
openSNPrs768638173
23andMers768638173
23andMe allrs768638173
SNP Nexus

SNPshotrs768638173
SNPdbers768638173
MSV3drs768638173
GWAS Ctlgrs768638173
Max Magnitude0
ClinVar
Risk rs768638173(T;T)
Alt rs768638173(T;T)
Reference rs768638173(C;C)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29553492C>T
CLNSRC
CLNACC RCV000168265.1,