Variant (rsID / SNP)

rs3779617

rs3779617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRHL2. Location: chromosome 8, position 102,631,911. Clinical significance in the table: Benign.

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Reference-table entries

GRHL2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:102631911
Cytoband: 8q22.3
HGVS: NM_024915.4(GRHL2):c.1243G>A (p.Val415Ile)
Allele change: Missense_V399I

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.