Variant (rsID / SNP)

rs139838162

rs139838162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFAP. Location: chromosome 17, position 42,992,542. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GFAPBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:42992542
Cytoband: 17q21.31
HGVS: NM_002055.5(GFAP):c.313C>T (p.Arg105Trp)
Allele change: Missense_R105W

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.