Variant (rsID / SNP)

rs3747690

rs3747690 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CWH43. Location: chromosome 4, position 48,988,450. The table records no clinical significance for this variant.

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Reference-table entries

CWH43Not classified

Variant type: missense_variant
Chromosome / position: 4:48988450
HGVS: NM_025087.3,c.4C>A,p.Pro2Thr
Allele change: Missense_P2T

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.