Variant (rsID / SNP)

rs140004406

rs140004406 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFAP. Location: chromosome 17, position 42,988,784. Clinical significance in the table: Likely benign.

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Reference-table entries

GFAPLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:42988784
Cytoband: 17q21.31
HGVS: NM_002055.5(GFAP):c.947G>A (p.Arg316Gln)
Allele change: Missense_R316Q

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.