Variant (rsID / SNP)

rs957680

rs957680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFM2. Location: chromosome 5, position 74,055,209. Clinical significance in the table: Benign.

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Reference-table entries

GFM2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:74055209
Cytoband: 5q13.3
HGVS: NM_032380.5(GFM2):c.191A>G (p.Asn64Ser)
Allele change: Missense_N96S

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.