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rs786203500

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203500(-;-)
Make rs786203500(-;TTATTACGAATTG)
Make rs786203500(TTATTACGAATTG;TTATTACGAATTG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31235949
GeneNF1
is asnp
is mentioned by
dbSNPrs786203500
ebirs786203500
HLIrs786203500
Exacrs786203500
Varsomers786203500
Maprs786203500
PheGenIrs786203500
hapmaprs786203500
1000 genomesrs786203500
hgdprs786203500
ensemblrs786203500
gopubmedrs786203500
geneviewrs786203500
scholarrs786203500
googlers786203500
pharmgkbrs786203500
gwascentralrs786203500
openSNPrs786203500
23andMers786203500
23andMe allrs786203500
SNP Nexus

SNPshotrs786203500
SNPdbers786203500
MSV3drs786203500
GWAS Ctlgrs786203500
Max Magnitude0
ClinVar
Risk rs786203500(TTATTACGAATTG;TTATTACGAATTG)
Alt rs786203500(TTATTACGAATTG;TTATTACGAATTG)
Reference rs786203500(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29562967_29562968insTTATTACGAATTG
CLNSRC
CLNACC RCV000166831.1,