Variant (rsID / SNP)

rs11102930

rs11102930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NGF. Location: chromosome 1, position 115,881,055. Clinical significance in the table: Benign.

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Reference-table entries

NGFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:115881055
Cytoband: 1p13.2
HGVS: NM_002506.2(NGF):c.-367C>T

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.