Variant (rsID / SNP)

rs814501

rs814501 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN4. Location: chromosome 19, position 41,038,574. The table records no clinical significance for this variant.

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Reference-table entries

SPTBN4Not classified

Variant type: missense_variant
Chromosome / position: 19:41038574
HGVS: NM_020971.3,c.3991G>A,p.Gly1331Ser
Allele change: Missense_G1331S

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.