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rs876658207

From SNPedia

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Geno Mag Summary
(TAGC;TAGC) 0 common in clinvar
Make rs876658207(-;-)
Make rs876658207(-;TAGC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31229204
GeneNF1
is asnp
is mentioned by
dbSNPrs876658207
ebirs876658207
HLIrs876658207
Exacrs876658207
Varsomers876658207
Maprs876658207
PheGenIrs876658207
hapmaprs876658207
1000 genomesrs876658207
hgdprs876658207
ensemblrs876658207
gopubmedrs876658207
geneviewrs876658207
scholarrs876658207
googlers876658207
pharmgkbrs876658207
gwascentralrs876658207
openSNPrs876658207
23andMers876658207
23andMe allrs876658207
SNP Nexus

SNPshotrs876658207
SNPdbers876658207
MSV3drs876658207
GWAS Ctlgrs876658207
Max Magnitude0
ClinVar
Risk rs876658207(;)
Alt rs876658207(;)
Reference rs876658207(TAGC;TAGC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene NF1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.29556222_29556225delTAGC
CLNSRC
CLNACC RCV000218184.1,