Variant (rsID / SNP)

rs41301291

rs41301291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF3. Location: chromosome 1, position 117,127,417. Clinical significance in the table: Benign.

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Reference-table entries

IGSF3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:117127417
Cytoband: 1p13.1
HGVS: NM_001007237.3(IGSF3):c.2698G>A (p.Val900Met)
Allele change: Missense_V900M

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.