Variant (rsID / SNP)

rs3796547

rs3796547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRACD. Location: chromosome 4, position 57,181,995. The table records no clinical significance for this variant.

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Reference-table entries

CRACDNot classified

Variant type: missense_variant
Chromosome / position: 4:57181995
HGVS: NM_001393381.1,c.2327C>T,p.Ser776Leu
Allele change: Missense_S776L

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.