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rs786202112

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202112(A;A)
Make rs786202112(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31327839
GeneNF1
is asnp
is mentioned by
dbSNPrs786202112
ebirs786202112
HLIrs786202112
Exacrs786202112
Varsomers786202112
Maprs786202112
PheGenIrs786202112
hapmaprs786202112
1000 genomesrs786202112
hgdprs786202112
ensemblrs786202112
gopubmedrs786202112
geneviewrs786202112
scholarrs786202112
googlers786202112
pharmgkbrs786202112
gwascentralrs786202112
openSNPrs786202112
23andMers786202112
23andMe allrs786202112
SNP Nexus

SNPshotrs786202112
SNPdbers786202112
MSV3drs786202112
GWAS Ctlgrs786202112
Max Magnitude0
ClinVar
Risk rs786202112(A;A)
Alt rs786202112(A;A)
Reference rs786202112(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29654857G>A
CLNSRC
CLNACC RCV000164762.1,