Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 9:108899816 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS011046 ; PhenCode IPNMDB_513 (A/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NG_008788.1:g.39513T>C_1269711014

This variation has 5 HGVS names - click the plus to show

9:g.108899816A>G
ENST00000537196.1:c.1157+6T>C
ENST00000374647.7:c.2204+6T>C
LRG_251:g.39513T>C
LRG_251t1.1:c.2204+6T>C

Variation displays