Variant (rsID / SNP)

rs1126642

rs1126642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFAP. Location: chromosome 17, position 42,989,063. Clinical significance in the table: Benign.

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Reference-table entries

GFAPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:42989063
Cytoband: 17q21.31
HGVS: NM_002055.5(GFAP):c.883G>A (p.Asp295Asn)
Allele change: Missense_D295N

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.